> top > docs > PubMed:26994442 > spans > 0-240 > annotations

PubMed:26994442 / 0-240 JSONTXT

Annnotations TAB JSON ListView MergeView

c_corpus

Id Subject Object Predicate Lexical cue
T2 22-25 CHEBI:16768 denotes MSH
T6 22-25 D009074 denotes MSH
T7 22-25 D009074 denotes MSH
T8 22-26 PR:O65607 denotes MSH3
T9 22-26 PR:000010667 denotes MSH3
T10 22-26 PR:Q59Y41 denotes MSH3
T11 22-26 PR:P25336 denotes MSH3
T12 22-26 PR:P20585 denotes MSH3
T13 22-26 PR:P26359 denotes MSH3
T14 22-26 PR:P13705 denotes MSH3
T15 22-26 PR:Q1ZXH0 denotes MSH3
T16 27-42 GO:0006298 denotes mismatch repair
T17 43-47 SO:0000704 denotes gene
T18 121-127 SO:0001068 denotes repeat
T21 141-144 SO:0000352 denotes DNA
T20 141-144 CHEBI:16991 denotes DNA
T22 141-144 D004247 denotes DNA
T19 141-144 GO:0005574 denotes DNA
T23 148-166 D009223 denotes myotonic dystrophy
T24 148-166 D009223 denotes myotonic dystrophy
T25 222-228 SO:0001068 denotes repeat

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
26994442-0#22#26#gene4437 22-26 gene4437 denotes MSH3
26994442-0#148#166#diseaseC0027126 148-166 diseaseC0027126 denotes myotonic dystrophy
22#26#gene4437148#166#diseaseC0027126 26994442-0#22#26#gene4437 26994442-0#148#166#diseaseC0027126 associated_with MSH3,myotonic dystrophy