LitCoin-MeSH-Disease-2  

PubMed:18366737 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue ID:
T1 93-97 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T2 99-104 DiseaseOrPhenotypicFeature denotes HLRCC DISEASE
T3 106-111 DiseaseOrPhenotypicFeature denotes tumor D009369
T4 112-120 DiseaseOrPhenotypicFeature denotes syndrome D013577
T5 136-155 DiseaseOrPhenotypicFeature denotes fumarase deficiency C538191
T6 389-405 DiseaseOrPhenotypicFeature denotes deficiency of FH DISEASE
T7 437-451 DiseaseOrPhenotypicFeature denotes encephalopathy D001927
T8 475-484 DiseaseOrPhenotypicFeature denotes Leiomyoma D007889
T9 562-603 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas DISEASE
T10 606-610 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T11 612-623 DiseaseOrPhenotypicFeature denotes OMIM 150800 DISEASE
T12 643-660 DiseaseOrPhenotypicFeature denotes renal cell cancer D002292
T13 733-780 DiseaseOrPhenotypicFeature denotes hereditary leiomyomatosis and renal cell cancer C535516
T14 782-787 DiseaseOrPhenotypicFeature denotes HLRCC DISEASE
T15 789-800 DiseaseOrPhenotypicFeature denotes OMIM 605839 DISEASE
T16 833-838 DiseaseOrPhenotypicFeature denotes tumor D009369
T17 1060-1073 DiseaseOrPhenotypicFeature denotes tumorigenesis D063646
T18 1723-1736 DiseaseOrPhenotypicFeature denotes FH deficiency DISEASE
T19 1764-1768 DiseaseOrPhenotypicFeature denotes MCUL DISEASE
T20 1769-1774 DiseaseOrPhenotypicFeature denotes HLRRC DISEASE
T21 2475-2484 DiseaseOrPhenotypicFeature denotes syndromes D013577