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PubMed:18366737 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue mondo_id
T1 4-6 DiseaseOrPhenotypicFeature denotes FH 0016525
T2 93-97 DiseaseOrPhenotypicFeature denotes MCUL 0007888
T3 99-104 DiseaseOrPhenotypicFeature denotes HLRCC 0007888
T4 106-120 DiseaseOrPhenotypicFeature denotes tumor syndrome 0021058
T5 136-155 DiseaseOrPhenotypicFeature denotes fumarase deficiency 0011730
T6 217-219 DiseaseOrPhenotypicFeature denotes FH 0016525
T7 403-405 DiseaseOrPhenotypicFeature denotes FH 0016525
T8 475-484 DiseaseOrPhenotypicFeature denotes Leiomyoma 0001572
T9 542-544 DiseaseOrPhenotypicFeature denotes FH 0016525
T10 562-603 DiseaseOrPhenotypicFeature denotes multiple cutaneous and uterine leiomyomas 0007888
T11 606-610 DiseaseOrPhenotypicFeature denotes MCUL 0007888
T12 643-660 DiseaseOrPhenotypicFeature denotes renal cell cancer 0003007|0005549
T14 733-780 DiseaseOrPhenotypicFeature denotes hereditary leiomyomatosis and renal cell cancer 0007888
T15 782-787 DiseaseOrPhenotypicFeature denotes HLRCC 0007888
T16 825-827 DiseaseOrPhenotypicFeature denotes FH 0016525
T17 833-838 DiseaseOrPhenotypicFeature denotes tumor 0005070
T18 1092-1094 DiseaseOrPhenotypicFeature denotes FH 0016525
T19 1444-1446 DiseaseOrPhenotypicFeature denotes FH 0016525
T20 1655-1657 DiseaseOrPhenotypicFeature denotes FH 0016525
T21 1723-1725 DiseaseOrPhenotypicFeature denotes FH 0016525
T22 1764-1768 DiseaseOrPhenotypicFeature denotes MCUL 0007888
T23 2052-2054 DiseaseOrPhenotypicFeature denotes FH 0016525
T24 2090-2092 DiseaseOrPhenotypicFeature denotes FH 0016525
T25 2176-2178 DiseaseOrPhenotypicFeature denotes FH 0016525
T26 2447-2449 DiseaseOrPhenotypicFeature denotes FH 0016525
T27 2475-2484 DiseaseOrPhenotypicFeature denotes syndromes 0002254