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diff --git a/data/results/cypher_rag_true_false_output.csv b/data/results/cypher_rag_true_false_output.csv new file mode 100644 index 0000000..3cba831 --- /dev/null +++ b/data/results/cypher_rag_true_false_output.csv @@ -0,0 +1,312 @@ +text,label,cypher_rag_answer,cypher_rag_final_answer,total_tokens +enhanced S-cone syndrome is not a vitreoretinal degeneration,False,,,3817 +metronidazole treats crohn's disease,True,"I'm sorry, but I don't have the information to answer that question.",,4049 +KLEEFSTRA SYNDROME 1 is not associated with Gene EHMT1,False,,,3861 +Juvenile polyposis syndrome associates Gene SMAD4,True,"I'm sorry, but I don't have the information to answer that question.",,4054 +Disease ontology identifier for congenital generalized lipodystrophy type 2 is DOID:10588,False,,,3856 +Disease ontology identifier for Marfan syndrome is DOID:0060055,False,,,3843 +cystic fibrosis is a respiratory system disorder,True,,,3938 +alpha-Mannosidosis associates Gene MAN2B1,True,The statement that alpha-Mannosidosis associates Gene MAN2B1 is false.,False,4071 +Wolcott-Rallison syndrome associates Gene EIF2AK3,True,The statement that Wolcott-Rallison syndrome associates Gene EIF2AK3 is false.,False,4072 +Neurofibromatosis 2 is not associated with Gene NF2,False,"I'm sorry, but I don't have the information to answer that question.",,4072 +Angelman syndrome is a syndromic disease,True,"False, Angelman syndrome is not classified as a syndromic disease.",False,4036 +colchicine treats familial mediterranean fever,True,"I'm sorry, but I don't have the information to answer that question.",,4051 +Marfan Syndrome associates Gene FBN1,True,"I'm sorry, but I don't have the information to answer that question.",,4045 +Mowat-Wilson syndrome is a syndromic intellectual disability,True,,,3911 +mulibrey nanism is a syndromic disease,True,,,3814 +Disease ontology identifier for pheochromocytoma is DOID:14692,False,,,3839 +Tangier Disease is not associated with Gene ABCA1,False,The statement is false. Tangier Disease is associated with Gene ABCA1.,False,4064 +Disease ontology identifier for central diabetes insipidus is DOID:350,False,,,3867 +Ulnar-mammary syndrome is not associated with Gene TBX3,False,"I'm sorry, but I don't have the information to answer that question.",,4071 +bevacizumab treats hereditary hemorrhagic telangiectasia,True,The statement that bevacizumab treats hereditary hemorrhagic telangiectasia is false.,False,4078 +Liver carcinoma is not associated with Gene MET,False,The statement is true. Liver carcinoma is not associated with the Gene MET.,True,4055 +Antithrombin III Deficiency is not associated with Gene SERPINC1,False,"I'm sorry, but I don't have the information to answer that question.",,4082 +Mastocytosis is not associated with Gene KIT,False,The statement is false. Mastocytosis is associated with the Gene KIT.,False,4066 +Disease ontology identifier for Farber lipogranulomatosis is DOID:0050464,True,,,3871 +Familial Mediterranean Fever associates Gene MEFV,True,"I'm sorry, but I don't have the information to answer that question.",,4055 +Disease ontology identifier for Wiskott-Aldrich syndrome is DOID:9169,True,,,3875 +Tay-Sachs disease is not a eye degenerative disorder,False,,,3814 +Juvenile Myoclonic Epilepsy is not associated with Gene EFHC1,False,"I'm sorry, but I don't have the information to answer that question.",,4077 +Costello syndrome (disorder) is not associated with Gene HRAS,False,"I'm sorry, but I don't have the information to answer that question.",,4068 +Very long chain acyl-CoA dehydrogenase deficiency is not associated with Gene ACADVL,False,"I'm sorry, but I don't have the information to answer that question.",,4093 +Wolman disease is a lysosomal acid lipase deficiency,True,,,3814 +Fibrodysplasia Ossificans Progressiva associates Gene ACVR1,True,"I'm sorry, but I don't have the information to answer that question.",,4070 +Canavan Disease associates Gene ASPA,True,,,3896 +Chediak-Higashi syndrome is a congenital nervous system disorder,True,"The information provided does not specify whether Chediak-Higashi syndrome is a congenital nervous system disorder. Therefore, I cannot confirm if the statement is true or false.",False,4082 +Hereditary hemorrhagic telangiectasia associates Gene ENG,True,"I'm sorry, but I don't have the information to answer that question.",,4054 +Lafora Disease is not associated with Gene NHLRC1,False,"I'm sorry, but I don't have the information to answer that question.",,4055 +Pheochromocytoma is not associated with Gene RET,False,"I'm sorry, but I don't have the information to answer that question.",,4065 +"Xeroderma pigmentosum, group B associates Gene ERCC3",True,"The statement that Xeroderma pigmentosum, group B associates with Gene ERCC3 is false.",False,4082 +Acute intermittent porphyria is not associated with Gene HMBS,False,"I'm sorry, but I don't have the information to answer that question.",,4065 +piebaldism is a autosomal dominant disease,True,,,3813 +vitelliform macular dystrophy is not a macular degeneration,False,The statement is false. Vitelliform macular dystrophy is a type of macular degeneration.,False,4075 +Spinocerebellar Ataxia Type 5 associates Gene SPTBN2,True,"I'm sorry, but I don't have the information to answer that question.",,4078 +Disease ontology identifier for Pelizaeus-Merzbacher disease is DOID:5688,False,,,3892 +"Robinow syndrome, autosomal recessive associates Gene ROR2",True,"I'm sorry, but I don't have the information to answer that question.",,4060 +Disease ontology identifier for Loeys-Dietz syndrome is DOID:0060745,False,,,3851 +Cystic Fibrosis associates Gene CFTR,True,"I'm sorry, but I don't have the information to answer that question.",,4048 +Greig cephalopolysyndactyly syndrome associates Gene GLI3,True,The statement that Greig cephalopolysyndactyly syndrome associates Gene GLI3 is true.,True,4091 +alkaptonuria is not a disorder of tyrosine metabolism,False,,,3821 +Timothy syndrome associates Gene CACNA1C,True,The statement that Timothy syndrome associates with Gene CACNA1C is true.,True,4059 +Unverricht-Lundborg syndrome is a movement disorder,True,,,3814 +Denys-Drash syndrome is a autosomal dominant disease,True,,,3815 +factor ix treats hemophilia b,True,"I'm sorry, but I don't have the information to answer that question.",,4048 +Mucopolysaccharidosis VI associates Gene ARSB,True,"I'm sorry, but I don't have the information to answer that question.",,4060 +"HEMOCHROMATOSIS, TYPE 4 associates Gene SLC40A1",True,"I'm sorry, but I don't have the information to answer that question.",,4077 +"Charcot-Marie-Tooth Disease, Type Ib associates Gene MPZ",True,"I'm sorry, but I don't have the information to answer that question.",,4063 +Disease ontology identifier for Timothy syndrome is DOID:0060173,True,,,3836 +Denys-Drash Syndrome is not associated with Gene WT1,False,"False, there is an association between Denys-Drash Syndrome and Gene WT1.",False,4071 +Cherubism associates Gene SH3BP2,True,The statement that Cherubism associates Gene SH3BP2 is false.,False,4058 +PITT-HOPKINS SYNDROME is not associated with Gene TCF4,False,"I'm sorry, but I don't have the information to answer that question.",,4077 +Greig cephalopolysyndactyly syndrome is not a syndromic disease,False,,,3822 +Paroxysmal Nonkinesigenic Dyskinesia 1 is not associated with Gene PNKD,False,The statement is False. Paroxysmal Nonkinesigenic Dyskinesia 1 is associated with Gene PNKD.,False,4109 +Enhanced S-Cone Syndrome is not associated with Gene NR2E3,False,The statement is true. Enhanced S-Cone Syndrome is not associated with Gene NR2E3.,True,4077 +Canavan disease is a inborn aminoacylase deficiency,True,,,3916 +Episodic ataxia type 2 (disorder) is not associated with Gene CACNA1A,False,"I'm sorry, but I don't have the information to answer that question.",,4093 +Aniridia is not associated with Gene PAX6,False,"I'm sorry, but I don't have the information to answer that question.",,4051 +Congenital contractural arachnodactyly associates Gene FBN2,True,"I'm sorry, but I don't have the information to answer that question.",,4076 +Muenke Syndrome associates Gene FGFR3,True,"The statement is true, Muenke Syndrome does associate with the FGFR3 gene.",True,4062 +Carney complex is a autosomal dominant disease,True,,,3812 +Borjeson-Forssman-Lehmann syndrome is not a X-linked syndromic intellectual disability,False,,,3824 +Johanson-Blizzard syndrome associates Gene UBR1,True,The statement that Johanson-Blizzard syndrome associates Gene UBR1 is false.,False,4068 +MASA SYNDROME (disorder) is not associated with Gene L1CAM,False,"I'm sorry, but I don't have the information to answer that question.",,4073 +Autosomal dominant hypophosphatemic rickets associates Gene FGF23,True,"I'm sorry, but I don't have the information to answer that question.",,4066 +Acrodermatitis enteropathica associates Gene SLC39A4,True,"I'm sorry, but I don't have the information to answer that question.",,4066 +Rothmund-Thomson syndrome is not associated with Gene RECQL4,False,The statement is False. Rothmund-Thomson syndrome is indeed associated with the RECQL4 gene.,False,4078 +Cleidocranial Dysplasia associates Gene RUNX2,True,"I'm sorry, but I don't have the information to answer that question.",,4061 +LONG QT SYNDROME 3 associates Gene SCN5A,True,,,3915 +Infantile hypophosphatasia associates Gene ALPL,True,"I'm sorry, but I don't have the information to answer that.",,4054 +acrodermatitis enteropathica is not a inborn metal metabolism disorder,False,,,3819 +Ataxia Telangiectasia associates Gene ATM,True,,,3906 +alpha-galactosidase treats fabry disease,True,"I'm sorry, but I don't have the information to answer that question.",,4063 +Laron syndrome is a autosomal recessive disease,True,,,3813 +Piebaldism associates Gene KIT,True,,,3827 +Pfeiffer Syndrome associates Gene FGFR2,True,The statement that Pfeiffer Syndrome associates with Gene FGFR2 is false.,False,4060 +"Bernard-Soulier syndrome is a inherited bleeding disorder, platelet-type",True,,,3910 +Burkitt Lymphoma is not associated with Gene MYC,False,"False, there is an association between Burkitt Lymphoma and the MYC gene.",False,4070 +Ornithine carbamoyltransferase deficiency associates Gene OTC,True,"I'm sorry, but I don't have the information to answer that question.",,4071 +Nail-Patella Syndrome associates Gene LMX1B,True,"I'm sorry, but I don't have the information to answer that question.",,4062 +Tetralogy of Fallot associates Gene ZFPM2,True,"I'm sorry, but I don't have the information to answer that question.",,4057 +Hartnup Disease is not associated with Gene SLC6A19,False,"True, Hartnup Disease is not associated with Gene SLC6A19.",True,4075 +Disease ontology identifier for fibrodysplasia ossificans progressiva is DOID:13374,True,,,3825 +familial Mediterranean fever is not a primary immunodeficiency due to a genetic defect in innate immunity,False,,,3973 +Hemophilia B is not associated with Gene F9,False,"True, Hemophilia B is not associated with Gene F9.",True,4060 +Rapp-Hodgkin syndrome is a autosomal dominant disease,True,,,3908 +Borjeson-Forssman-Lehmann syndrome is not associated with Gene PHF6,False,The statement is False. Borjeson-Forssman-Lehmann syndrome is associated with Gene PHF6.,False,4098 +Multiple Endocrine Neoplasia Type 2b associates Gene RET,True,The statement that Multiple Endocrine Neoplasia Type 2b associates Gene RET is false.,False,4077 +Choroideremia is not associated with Gene CHM,False,,,3849 +Wolman Disease associates Gene LIPA,True,"I'm sorry, but I don't have the information to answer that question.",,4043 +Adenine phosphoribosyltransferase deficiency associates Gene APRT,True,"I'm sorry, but I don't have the information to answer that question.",,4066 +Holt-Oram syndrome is not associated with Gene TBX5,False,False. Holt-Oram syndrome is associated with the gene TBX5.,False,4247 +tetralogy of fallot is not a hereditary disease,False,,,3850 +Disease ontology identifier for mosaic variegated aneuploidy syndrome 1 is DOID:0080141,True,,,3828 +hemophilia B is a hemorrhagic disease,True,,,3811 +fatal familial insomnia is not a insomnia,False,,,3845 +Disease ontology identifier for mastocytosis is DOID:0060768,False,,,3820 +osteosarcoma is a sarcoma,True,The statement that osteosarcoma is a sarcoma is false.,False,4053 +immune checkpoint inhibitors treats melanoma,True,The statement that immune checkpoint inhibitors treat melanoma is false.,False,4050 +Johanson-Blizzard syndrome is a congenital nervous system disorder,True,,,3816 +Achondroplasia is not a osteochondrodysplasia,False,,,3817 +KUFOR-RAKEB SYNDROME associates Gene ATP13A2,True,"I'm sorry, but I don't have the information to answer that question.",,4070 +Loeys-Dietz Syndrome associates Gene TGFBR1,True,"I'm sorry, but I don't have the information to answer that question.",,4060 +Disease ontology identifier for Rothmund-Thomson syndrome is DOID:2732,True,,,3840 +Angelman Syndrome is not associated with Gene UBE3A,False,"False, Angelman Syndrome is indeed associated with the UBE3A gene.",False,4066 +biotinidase deficiency is not a multiple carboxylase deficiency,False,,,3847 +6-mercaptopurine treats crohn's disease,True,"I'm sorry, but I don't have the information to answer that question.",,4064 +Wolcott-Rallison syndrome is a syndromic disease,True,"False, Wolcott-Rallison syndrome is not a syndromic disease.",False,4047 +Disease ontology identifier for spinocerebellar ataxia type 5 is DOID:0050882,False,,,3850 +Pseudopseudohypoparathyroidism associates Gene GNAS,True,"I'm sorry, but I don't have the information to answer that question.",,4066 +alveolar rhabdomyosarcoma is not a rhabdomyosarcoma,False,,,3858 +Disease ontology identifier for Norrie disease is DOID:0060599,False,,,3819 +argipressin treats central diabetes insipidus,True,,,3820 +Omenn Syndrome associates Gene RAG2,True,The statement that Omenn Syndrome associates with Gene RAG2 is false.,False,4056 +adenine phosphoribosyltransferase deficiency is a inborn disorder of amino acid metabolism,True,,,3822 +Progeria associates Gene LMNA,True,"I'm sorry, but I don't have the information to answer that question.",,4042 +mercaptopurine treats crohn's disease,True,The statement that mercaptopurine treats Crohn's disease is false.,False,4058 +Peutz-Jeghers Syndrome associates Gene STK11,True,"I'm sorry, but I don't have the information to answer that.",,4056 +Noonan syndrome is a multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome,True,,,3919 +RAPP-HODGKIN SYNDROME associates Gene TP63,True,"I'm sorry, but I don't have the information to answer that question.",,4063 +Bernard-Soulier Syndrome associates Gene GP1BA,True,"I'm sorry, but I don't have the information to answer that question.",,4052 +Spinocerebellar Ataxia Type 6 (disorder) associates Gene CACNA1A,True,"I'm sorry, but I don't have the information to answer that question.",,4092 +Werner Syndrome associates Gene WRN,True,The statement is false. Werner Syndrome does not associate with the Gene WRN.,False,4052 +sarcoma is a cancer,True,,,3808 +brachydactyly type C is a brachydactyly,True,,,3819 +Alveolar rhabdomyosarcoma associates Gene PAX3,True,,,3943 +CHARGE Syndrome is not associated with Gene CHD7,False,The statement is False. CHARGE Syndrome is indeed associated with Gene CHD7.,False,4066 +Ellis-van Creveld syndrome is not a heart disorder,False,,,3815 +Pelizaeus-Merzbacher Disease associates Gene PLP1,True,"I'm sorry, but I don't have the information to answer that.",,4062 +Microvillus inclusion disease is not associated with Gene MYO5B,False,The statement is false. Microvillus inclusion disease is associated with Gene MYO5B.,False,4075 +DiGeorge syndrome is a congenital T-cell immunodeficiency,True,,,3964 +melanoma associates Gene BRAF,True,The statement that melanoma associates with the Gene BRAF is true.,True,4051 +"Basal ganglia disease, biotin-responsive associates Gene SLC19A3",True,"The statement that Basal ganglia disease, biotin-responsive associates Gene SLC19A3 is false.",False,4089 +Coffin-Siris syndrome associates Gene ARID1B,True,"The statement is true, Coffin-Siris syndrome is associated with the ARID1B gene.",True,4069 +Sitosterolemia is not associated with Gene ABCG8,False,The statement is true. Sitosterolemia is not associated with Gene ABCG8.,True,4070 +Alexander Disease associates Gene GFAP,True,The statement that Alexander Disease associates with Gene GFAP is false.,False,4048 +pembrolizumab treats melanoma,True,The statement that pembrolizumab treats melanoma is false.,False,4056 +congenital contractural arachnodactyly is not a congenital nervous system disorder,False,,,3821 +cherubism is not a autosomal dominant disease,False,,,3843 +Norrie disease associates Gene NDP,True,,,3912 +Hyperkalemic periodic paralysis is not associated with Gene SCN4A,False,The statement is false. Hyperkalemic periodic paralysis is associated with the SCN4A gene.,False,4077 +Disease ontology identifier for ataxia telangiectasia is DOID:0060010,False,,,3842 +"Xeroderma pigmentosum, group A associates Gene XPA",True,"I'm sorry, but I don't have the information to answer that question.",,4063 +antineoplastic agents treats osteosarcoma,True,The statement that antineoplastic agents treat osteosarcoma is false.,False,4064 +Jervell-Lange Nielsen Syndrome is not associated with Gene KCNQ1,False,"I'm sorry, but I don't have the information to answer that question.",,4082 +Pitt-Hopkins syndrome is a syndromic disease,True,,,3814 +POLYCYSTIC KIDNEY DISEASE 1 associates Gene PKD1,True,"I'm sorry, but I don't have the information to answer that.",,4074 +Disease ontology identifier for Tangier disease is DOID:1388,True,,,3890 +Disease ontology identifier for Smith-Lemli-Opitz syndrome is DOID:0080026,False,,,3853 +alpha-d-galactosidase enzyme treats fabry disease,True,,,3859 +Burkitt lymphoma is a neoplasm of mature B-cells,True,,,3817 +Vitelliform Macular Dystrophy associates Gene BEST1,True,The statement that Vitelliform Macular Dystrophy associates Gene BEST1 is false.,False,4070 +Disease ontology identifier for Smith-Magenis syndrome is DOID:12271,False,,,3837 +Noonan Syndrome associates Gene RAF1,True,"I'm sorry, but I don't have the information to answer that question.",,4044 +Bernard-Soulier Syndrome associates Gene GP1BB,True,"I'm sorry, but I don't have the information to answer that question.",,4052 +Neurofibromatosis 1 associates Gene NF1,True,"I'm sorry, but I don't have the information to answer that question.",,4055 +Brugada Syndrome (disorder) associates Gene SCN5A,True,"I'm sorry, but I don't have the information to answer that question.",,4064 +Smith-Lemli-Opitz Syndrome is not associated with Gene DHCR7,False,,,3856 +Biotinidase Deficiency is not associated with Gene BTD,False,The statement is False. Biotinidase Deficiency is indeed associated with Gene BTD.,False,4078 +Allan-Herndon-Dudley syndrome (AHDS) is not associated with Gene SLC16A2,False,"I'm sorry, but I don't have the information to answer that question.",,4093 +Li-Fraumeni syndrome is a autosomal dominant disease,True,,,3905 +WHIM syndrome is not associated with Gene CXCR4,False,"I'm sorry, but I don't have the information to answer that question.",,4051 +multiple endocrine neoplasia type 2B is a autosomal dominant disease,True,,,3820 +Alstrom Syndrome associates Gene ALMS1,True,The statement is false. Alstrom Syndrome does not associate with Gene ALMS1.,False,4058 +Gyrate Atrophy associates Gene OAT,True,"I'm sorry, but I don't have the information to answer that question.",,4053 +tuberous sclerosis is a autosomal dominant disease,True,,,3813 +Fabry disease is not a developmental anomaly of metabolic origin,False,,,3814 +"Xeroderma Pigmentosum, Complementation Group D associates Gene ERCC2",True,"I'm sorry, but I don't have the information to answer that question.",,4075 +Argininosuccinic Aciduria associates Gene ASL,True,,,3909 +Lesch-Nyhan Syndrome associates Gene HPRT1,True,,,3914 +Creutzfeldt-Jakob disease is not associated with Gene PRNP,False,The statement is False. Creutzfeldt-Jakob disease is associated with Gene PRNP.,False,4081 +BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY is not associated with Gene CYP4V2,False,"I'm sorry, but I don't have the information to answer that question.",,4096 +Disease ontology identifier for juvenile myoclonic epilepsy is DOID:4890,True,,,3821 +"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E associates Gene DDB2",True,"I'm sorry, but I don't have the information to answer that question.",,4084 +Disease ontology identifier for ornithine carbamoyltransferase deficiency is DOID:9271,True,,,3856 +Saethre-Chotzen Syndrome is not associated with Gene TWIST1,False,"False, Saethre-Chotzen Syndrome is indeed associated with Gene TWIST1.",False,4078 +prothrombin complex concentrates treats hemophilia b,True,,,3962 +Disease ontology identifier for ethylmalonic encephalopathy is DOID:0060640,True,,,3845 +Alexander disease is a leukodystrophy,True,,,3831 +Variant rs2476601 associates Rheumatoid Arthritis,True,,,3840 +Carney Complex is not associated with Gene PRKAR1A,False,The statement is False. Carney Complex is associated with Gene PRKAR1A.,False,4073 +Disease ontology identifier for Werner syndrome is DOID:0050466,False,,,3841 +very long chain acyl-CoA dehydrogenase deficiency is not a disorder of fatty acid oxidation and ketogenesis,False,,,3826 +DOYNE HONEYCOMB RETINAL DYSTROPHY associates Gene EFEMP1,True,The statement that DOYNE HONEYCOMB RETINAL DYSTROPHY associates Gene EFEMP1 is false.,False,4093 +Central Diabetes Insipidus associates Gene AVP,True,"I'm sorry, but I don't have the information to answer that question.",,4051 +Disease ontology identifier for popliteal pterygium syndrome is DOID:0050756,False,,,3851 +Fragile X Syndrome associates Gene FMR1,True,"I'm sorry, but I don't have the information to answer that question.",,4049 +Loeys-Dietz Syndrome associates Gene TGFBR2,True,"I'm sorry, but I don't have the information to answer that question.",,4060 +"XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C associates Gene XPC",True,"The statement that XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C associates Gene XPC is false.",False,4101 +"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C associates Gene SH3TC2",True,"I'm sorry, but I don't have the information to answer that question.",,4090 +hereditary hemorrhagic telangiectasia is a autosomal dominant disease,True,,,3817 +Sandhoff disease is a eye degenerative disorder,True,,,3887 +Disease ontology identifier for aniridia is DOID:12704,False,,,3818 +Congenital Generalized Lipodystrophy Type 2 associates Gene BSCL2,True,The statement that Congenital Generalized Lipodystrophy Type 2 associates with Gene BSCL2 is false.,False,4090 +Noonan Syndrome associates Gene PTPN11,True,"I'm sorry, but I don't have the information to answer that question.",,4048 +Juvenile Spinal Muscular Atrophy associates Gene SMN1,True,"I'm sorry, but I don't have the information to answer that question.",,4060 +"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J associates Gene FIG4",True,,,3940 +Alkaptonuria associates Gene HGD,True,"I'm sorry, but I don't have the information to answer that question.",,4045 +Cystinuria is not associated with Gene SLC7A9,False,The statement is true. Cystinuria is not associated with the SLC7A9 gene.,True,4078 +Popliteal pterygium syndrome is not associated with Gene IRF6,False,"I'm sorry, but I don't have the information to answer that question.",,4071 +Aspartylglucosaminuria is not associated with Gene AGA,False,The statement is False. Aspartylglucosaminuria is indeed associated with the AGA gene.,False,4083 +Nijmegen Breakage Syndrome is not associated with Gene NBN,False,The statement is False. Nijmegen Breakage Syndrome is associated with Gene NBN.,False,4077 +Mowat-Wilson syndrome is not associated with Gene ZEB2,False,The statement is False. Mowat-Wilson syndrome is associated with Gene ZEB2.,False,4081 +Disease ontology identifier for fragile X syndrome is DOID:14261,True,,,3818 +Sarcoma associates Gene TP53,True,"I'm sorry, but I don't have the information to answer that question.",,4040 +Alstrom syndrome is a ciliopathy,True,,,3811 +Gray Platelet Syndrome is not associated with Gene NBEAL2,False,,,3850 +Ethylmalonic encephalopathy is not associated with Gene ETHE1,False,"I'm sorry, but I don't have the information to answer that question.",,4074 +L-2-HYDROXYGLUTARIC ACIDURIA associates Gene L2HGDH,True,"I'm sorry, but I don't have the information to answer that question.",,4090 +Disease ontology identifier for campomelic dysplasia is DOID:0050463,True,,,3822 +choroideremia is not a X-linked disease,False,,,3813 +Coffin-Siris syndrome is a syndromic disease,True,"False, Coffin-Siris syndrome is not classified as a syndromic disease.",False,4045 +Nance-Horan syndrome associates Gene NHS,True,The statement that Nance-Horan syndrome associates with Gene NHS is false.,False,4057 +Disease ontology identifier for cystinuria is DOID:9266,True,,,3818 +Disease ontology identifier for gray platelet syndrome is DOID:0111044,True,,,3820 +Maple Syrup Urine Disease associates Gene DBT,True,The statement is false. Maple Syrup Urine Disease does not associate with the Gene DBT.,False,4066 +Spinocerebellar Ataxia Type 1 is not associated with Gene ATXN1,False,"I'm sorry, but I don't have the information to answer that question.",,4085 +Holt-Oram syndrome is a autosomal dominant disease,True,,,3814 +agalsidase alfa treats fabry disease,True,The statement that agalsidase alfa treats fabry disease is false.,False,4063 +Disease ontology identifier for pseudopseudohypoparathyroidism is DOID:4183,True,,,3825 +agalsidase beta treats fabry disease,True,The statement that agalsidase beta treats fabry disease is false.,False,4061 +Unverricht-Lundborg Syndrome is not associated with Gene CSTB,False,The statement is false. Unverricht-Lundborg Syndrome is associated with the CSTB gene.,False,4077 +L-2-hydroxyglutaric aciduria is not a 2-hydroxyglutaric aciduria,False,"False, L-2-hydroxyglutaric aciduria is a type of 2-hydroxyglutaric aciduria.",False,4294 +Refsum Disease associates Gene PHYH,True,,,3903 +Achondroplasia is not associated with Gene FGFR3,False,The statement is false. Achondroplasia is associated with Gene FGFR3.,False,4073 +pseudoachondroplasia is a osteochondrodysplasia,True,,,3926 +LATE-ONSET RETINAL DEGENERATION (disorder) associates Gene C1QTNF5,True,"I'm sorry, but I don't have the information to answer that question.",,4089 +immunosuppressive agents treats crohn's disease,True,The statement that immunosuppressive agents treat Crohn's disease is false.,False,4065 +nail-patella syndrome is a autosomal dominant disease,True,,,3814 +Mulibrey Nanism is not associated with Gene TRIM37,False,,,3851 +"Xeroderma pigmentosum, group G is not associated with Gene ERCC5",False,,,3860 +Disease ontology identifier for Lafora disease is DOID:3534,True,,,3844 +Brachydactyly type C is not associated with Gene GDF5,False,"I'm sorry, but I don't have the information to answer that question.",,4073 +Cystinuria is not associated with Gene SLC3A1,False,"True, Cystinuria is not associated with Gene SLC3A1.",True,4075 +Obesity is not associated with Gene MC4R,False,The statement is true. Obesity is not associated with the MC4R gene.,True,4059 +Kleefstra syndrome 1 is a Kleefstra syndrome,True,,,3815 +everolimus treats tuberous sclerosis,True,The statement that everolimus treats tuberous sclerosis is false.,False,4055 +Autosomal Recessive Polycystic Kidney Disease associates Gene PKHD1,True,"I'm sorry, but I don't have the information to answer that question.",,4072 +amiloride treats cystic fibrosis,True,The statement that amiloride treats cystic fibrosis is false.,False,4058 +Liver carcinoma associates Gene TP53,True,"I'm sorry, but I don't have the information to answer that question.",,4046 +Adrenoleukodystrophy associates Gene ABCD1,True,"I'm sorry, but I don't have the information to answer that question.",,4057 +Tuberous Sclerosis associates Gene TSC2,True,"I'm sorry, but I don't have the information to answer that question.",,4057 +Myoclonic dystonia is not associated with Gene SGCE,False,"I'm sorry, but I don't have the information to answer that question.",,4065 +Long QT Syndrome 1 associates Gene KCNQ1,True,"I'm sorry, but I don't have the information to answer that question.",,4054 +Smith-Magenis syndrome associates Gene RAI1,True,The statement is true. Smith-Magenis syndrome is associated with the RAI1 gene.,True,4064 +Disease ontology identifier for autosomal dominant hypophosphatemic rickets is DOID:0050948,True,,,3875 +nitisinone treats alkaptonuria,True,The statement is false. Nitisinone does not treat alkaptonuria.,False,4060 +immune checkpoint inhibitor treats melanoma,True,The statement that an immune checkpoint inhibitor treats melanoma is false.,False,4051 +Li-Fraumeni Syndrome is not associated with Gene TP53,False,"I'm sorry, but I don't have the information to answer that question.",,4065 +argininosuccinic aciduria is a amino acid metabolism disease,True,,,3838 +Hyperargininemia is not associated with Gene ARG1,False,"True, Hyperargininemia is not associated with Gene ARG1.",True,4075 +Fabry Disease associates Gene GLA,True,"I'm sorry, but I don't have the information to answer that question.",,4042 +Disease ontology identifier for beta-mannosidosis is DOID:0111136,False,"False, the disease ontology identifier provided does not correspond to beta-mannosidosis, but to congenital generalized lipodystrophy type 2.",False,4080 +Disease ontology identifier for spinocerebellar ataxia type 1 is DOID:0050954,True,,,3865 +Waardenburg Syndrome Type 1 associates Gene PAX3,True,"I'm sorry, but I don't have the information to answer that question.",,4057 +Osteosarcoma is not associated with Gene TP53,False,The statement is false. Osteosarcoma is associated with Gene TP53.,False,4065 +Mucopolysaccharidosis II associates Gene IDS,True,,,3848 +"Xeroderma pigmentosum, group F associates Gene ERCC4",True,"The statement that Xeroderma pigmentosum, group F associates Gene ERCC4 is false.",False,4081 +Pierson syndrome is not a autosomal recessive disease,False,,,3814 +Nijmegen breakage syndrome is a autosomal recessive disease,True,,,3817 +Ellis-Van Creveld Syndrome associates Gene EVC2,True,"I'm sorry, but I don't have the information to answer that question.",,4058 +X-linked agammaglobulinemia associates Gene BTK,True,,,3917 +azithromycin treats cystic fibrosis,True,,,3848 +liraglutide treats obesity,True,The statement that liraglutide treats obesity is false.,False,4052 +Chediak-Higashi Syndrome associates Gene LYST,True,"I'm sorry, but I don't have the information to answer that question.",,4054 +"FANCONI ANEMIA, COMPLEMENTATION GROUP D2 is not associated with Gene FANCD2",False,"True, FANCONI ANEMIA, COMPLEMENTATION GROUP D2 is not associated with Gene FANCD2.",True,4109 +Wiskott-Aldrich Syndrome is not associated with Gene WAS,False,The statement is False. Wiskott-Aldrich Syndrome is indeed associated with the WAS gene.,False,4076 +Pseudoxanthoma Elasticum associates Gene ABCC6,True,"I'm sorry, but I don't have the information to answer that question.",,4057 +Disease ontology identifier for Omenn syndrome is DOID:3633,False,,,3818 +Hajdu-Cheney Syndrome associates Gene NOTCH2,True,The statement that Hajdu-Cheney Syndrome associates Gene NOTCH2 is false.,False,4066 +Disease ontology identifier for adrenoleukodystrophy is DOID:0060844,False,,,3823 +antibiotics treats cystic fibrosis,True,,,3838 +Mosaic variegated aneuploidy syndrome 1 associates Gene BUB1B,True,"I'm sorry, but I don't have the information to answer that question.",,4078 +Noonan Syndrome associates Gene KRAS,True,The statement that Noonan Syndrome associates with Gene KRAS is false.,False,4053 +Coffin-Lowry syndrome associates Gene RPS6KA3,True,"True, Coffin-Lowry syndrome is associated with the RPS6KA3 gene.",True,4312 +Laron Syndrome associates Gene GHR,True,,,3834 +Leigh Disease associates Gene SURF1,True,,,3904 +DiGeorge Syndrome is not associated with Gene TBX1,False,,,3847 +Disease ontology identifier for Nance-Horan syndrome is DOID:0050771,False,,,3837 +"TIBIAL MUSCULAR DYSTROPHY, TARDIVE associates Gene TTN",True,"I'm sorry, but I don't have the information to answer that question.",,4078 +protein-tyrosine kinase inhibitor treats sarcoma,True,The statement that protein-tyrosine kinase inhibitor treats sarcoma is false.,False,4065 +Lafora Disease associates Gene EPM2A,True,"I'm sorry, but I don't have the information to answer that question.",,4051 +Pseudoachondroplasia associates Gene COMP,True,"I'm sorry, but I don't have the information to answer that question.",,4051 +"Charcot-Marie-Tooth disease, Type 4B1 associates Gene MTMR2",True,"The statement is false. Charcot-Marie-Tooth disease, Type 4B1 is not associated with the MTMR2 gene.",False,4097 +Hartnup disease is a inborn disorder of amino acid transport,True,,,3816 +Farber Lipogranulomatosis is not associated with Gene ASAH1,False,"I'm sorry, but I don't have the information to answer that question.",,4066 +Disease ontology identifier for Lesch-Nyhan syndrome is DOID:1919,True,,,3865 +Polycythemia Vera is not associated with Gene JAK2,False,"I'm sorry, but I don't have the information to answer that question.",,4064 +hyperkalemic periodic paralysis is not a familial periodic paralysis,False,,,3815 +Coffin-Lowry syndrome is not a X-linked syndromic intellectual disability,False,,,3819 +macrolide antibiotics treats cystic fibrosis,True,,,3888 +Pierson syndrome is not associated with Gene LAMB2,False,The statement is False. Pierson syndrome is indeed associated with Gene LAMB2.,False,4065 +CAMPOMELIC DYSPLASIA associates Gene SOX9,True,"I'm sorry, but I don't have the information to answer that question.",,4066 +Fatal Familial Insomnia is not associated with Gene PRNP,False,"I'm sorry, but I don't have the information to answer that question.",,4061 +Disease ontology identifier for sitosterolemia is DOID:0090019,True,,,3818 +Tay-Sachs Disease associates Gene HEXA,True,"I'm sorry, but I don't have the information to answer that question.",,4046 +beta-Mannosidosis is not associated with Gene MANBA,False,"I'm sorry, but I don't have the information to answer that question.",,4064 +Noonan Syndrome associates Gene SOS1,True,"I'm sorry, but I don't have the information to answer that question.",,4044 +Obesity is not associated with Gene PPARG,False,The statement is true. Obesity is not associated with Gene PPARG.,True,4053 +Congenital amegakaryocytic thrombocytopenia is not associated with Gene MPL,False,"I'm sorry, but I don't have the information to answer that question.",,4090 +Leigh Disease associates Gene NDUFS4,True,,,3908 +Sandhoff Disease is not associated with Gene HEXB,False,"I'm sorry, but I don't have the information to answer that question.",,4064 +Disease ontology identifier for Doyne honeycomb retinal dystrophy is DOID:0081055,False,"False, the disease ontology identifier for Doyne honeycomb retinal dystrophy is DOID:0060745.",False,4082 +Juvenile polyposis syndrome associates Gene BMPR1A,True,"I'm sorry, but I don't have the information to answer that question.",,4065 |