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PubMed:10220146 JSONTXT

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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10220146-4#152#157#geners199472690 1120-1125 geners199472690 denotes F157C
10220146-4#125#129#diseaseC0023976 1093-1097 diseaseC0023976 denotes LQTS
152#157#geners199472690125#129#diseaseC0023976 10220146-4#152#157#geners199472690 10220146-4#125#129#diseaseC0023976 associated_with F157C,LQTS

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10220146-3#96#101#gene57162 640-645 gene57162 denotes PRISM
10220146-3#96#101#gene93166 640-645 gene93166 denotes PRISM
10220146-3#96#101#gene57162 640-645 gene57162 denotes PRISM
10220146-3#96#101#gene93166 640-645 gene93166 denotes PRISM
10220146-3#96#101#gene57162 640-645 gene57162 denotes PRISM
10220146-3#96#101#gene93166 640-645 gene93166 denotes PRISM
10220146-3#96#101#gene57162 640-645 gene57162 denotes PRISM
10220146-3#96#101#gene93166 640-645 gene93166 denotes PRISM
10220146-3#343#360#diseaseC0018799 887-904 diseaseC0018799 denotes cardiac disorders
10220146-3#361#377#diseaseC0023976 905-921 diseaseC0023976 denotes long QT syndrome
10220146-3#389#416#diseaseC0007194 933-960 diseaseC0007194 denotes hypertrophic cardiomyopathy
10220146-3#418#421#diseaseC0007194 962-965 diseaseC0007194 denotes HCM
10220146-4#161#167#gene3784 1129-1135 gene3784 denotes KVLQT1
10220146-4#181#185#gene3757 1149-1153 gene3757 denotes HERG
10220146-4#230#234#gene3757 1198-1202 gene3757 denotes HERG
10220146-4#239#243#gene4625 1207-1211 gene4625 denotes MYH7
10220146-4#125#129#diseaseC0023976 1093-1097 diseaseC0023976 denotes LQTS
96#101#gene57162343#360#diseaseC0018799 10220146-3#96#101#gene57162 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene57162361#377#diseaseC0023976 10220146-3#96#101#gene57162 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene57162389#416#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene57162418#421#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene93166343#360#diseaseC0018799 10220146-3#96#101#gene93166 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene93166361#377#diseaseC0023976 10220146-3#96#101#gene93166 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene93166389#416#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene93166418#421#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene57162343#360#diseaseC0018799 10220146-3#96#101#gene57162 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene57162361#377#diseaseC0023976 10220146-3#96#101#gene57162 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene57162389#416#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene57162418#421#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene93166343#360#diseaseC0018799 10220146-3#96#101#gene93166 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene93166361#377#diseaseC0023976 10220146-3#96#101#gene93166 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene93166389#416#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene93166418#421#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene57162343#360#diseaseC0018799 10220146-3#96#101#gene57162 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene57162361#377#diseaseC0023976 10220146-3#96#101#gene57162 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene57162389#416#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene57162418#421#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene93166343#360#diseaseC0018799 10220146-3#96#101#gene93166 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene93166361#377#diseaseC0023976 10220146-3#96#101#gene93166 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene93166389#416#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene93166418#421#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene57162343#360#diseaseC0018799 10220146-3#96#101#gene57162 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene57162361#377#diseaseC0023976 10220146-3#96#101#gene57162 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene57162389#416#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene57162418#421#diseaseC0007194 10220146-3#96#101#gene57162 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
96#101#gene93166343#360#diseaseC0018799 10220146-3#96#101#gene93166 10220146-3#343#360#diseaseC0018799 associated_with PRISM,cardiac disorders
96#101#gene93166361#377#diseaseC0023976 10220146-3#96#101#gene93166 10220146-3#361#377#diseaseC0023976 associated_with PRISM,long QT syndrome
96#101#gene93166389#416#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#389#416#diseaseC0007194 associated_with PRISM,hypertrophic cardiomyopathy
96#101#gene93166418#421#diseaseC0007194 10220146-3#96#101#gene93166 10220146-3#418#421#diseaseC0007194 associated_with PRISM,HCM
161#167#gene3784125#129#diseaseC0023976 10220146-4#161#167#gene3784 10220146-4#125#129#diseaseC0023976 associated_with KVLQT1,LQTS
181#185#gene3757125#129#diseaseC0023976 10220146-4#181#185#gene3757 10220146-4#125#129#diseaseC0023976 associated_with HERG,LQTS
230#234#gene3757125#129#diseaseC0023976 10220146-4#230#234#gene3757 10220146-4#125#129#diseaseC0023976 associated_with HERG,LQTS
239#243#gene4625125#129#diseaseC0023976 10220146-4#239#243#gene4625 10220146-4#125#129#diseaseC0023976 associated_with MYH7,LQTS

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1129-1135 gene:3784 denotes KVLQT1
T1 1093-1097 disease:C0023976 denotes LQTS
T2 1149-1153 gene:3757 denotes HERG
T3 1093-1097 disease:C0023976 denotes LQTS
T4 1198-1202 gene:3757 denotes HERG
T5 1093-1097 disease:C0023976 denotes LQTS
T6 1207-1211 gene:4625 denotes MYH7
T7 1093-1097 disease:C0023976 denotes LQTS
R1 T0 T1 associated_with KVLQT1,LQTS
R2 T2 T3 associated_with HERG,LQTS
R3 T4 T5 associated_with HERG,LQTS
R4 T6 T7 associated_with MYH7,LQTS

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 230-236 HP_0002664 denotes cancer
T2 887-904 HP_0001627 denotes cardiac disorders
T3 905-921 HP_0001657 denotes long QT syndrome
T4 933-960 HP_0001639 denotes hypertrophic cardiomyopathy
T5 946-960 HP_0001638 denotes cardiomyopathy