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PubMed:10200053 JSONTXT

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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10200053-2#41#47#geners137854600 355-361 geners137854600 denotes R1623Q
10200053-2#100#104#diseaseC0023976 414-418 diseaseC0023976 denotes LQTS
41#47#geners137854600100#104#diseaseC0023976 10200053-2#41#47#geners137854600 10200053-2#100#104#diseaseC0023976 associated_with R1623Q,LQTS

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10200053-6#60#65#gene6331 1009-1014 gene6331 denotes SCN5A
10200053-6#82#86#diseaseC0023976 1031-1035 diseaseC0023976 denotes LQTS
60#65#gene633182#86#diseaseC0023976 10200053-6#60#65#gene6331 10200053-6#82#86#diseaseC0023976 associated_with SCN5A,LQTS

DisGeNET

Id Subject Object Predicate Lexical cue
T0 226-231 gene:6331 denotes SCN5A
T1 263-279 disease:C0023976 denotes long QT syndrome
T2 226-231 gene:6331 denotes SCN5A
T3 281-285 disease:C0023976 denotes LQTS
T4 370-375 gene:6331 denotes SCN5A
T5 414-418 disease:C0023976 denotes LQTS
T6 1009-1014 gene:6331 denotes SCN5A
T7 1031-1035 disease:C0023976 denotes LQTS
R1 T0 T1 associated_with SCN5A,long QT syndrome
R2 T2 T3 associated_with SCN5A,LQTS
R3 T4 T5 associated_with SCN5A,LQTS
R4 T6 T7 associated_with SCN5A,LQTS

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 263-279 HP_0001657 denotes long QT syndrome