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PubMed:18272172 JSONTXT

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tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 261-270 DNAMutation:c|SUB|G|2398+1|C denotes 2398+1G>C
T2 397-406 DNAMutation:c|SUB|G|2398+1|C denotes 2398+1G>C
T3 618-627 DNAMutation:c|SUB|G|2398+1|C denotes 2398+1G>C
T4 1347-1356 DNAMutation:c|SUB|G|2398+1|C denotes 2398+1G>C

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
18272172-2#89#98#geners794728391 261-270 geners794728391 denotes 2398+1G>C
18272172-2#193#209#diseaseC0023976 365-381 diseaseC0023976 denotes long QT syndrome
89#98#geners794728391193#209#diseaseC0023976 18272172-2#89#98#geners794728391 18272172-2#193#209#diseaseC0023976 associated_with 2398+1G>C,long QT syndrome

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 66-82 DiseaseOrPhenotypicFeature denotes long QT syndrome 0002442
T2 154-170 DiseaseOrPhenotypicFeature denotes long QT syndrome 0002442
T3 365-381 DiseaseOrPhenotypicFeature denotes long QT syndrome 0002442
T4 1489-1495 DiseaseOrPhenotypicFeature denotes defect 0008568