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PubMed:20846357 JSONTXT 35 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue mondo_id
T1 102-111 DiseaseOrPhenotypicFeature denotes keratitis 0003085
T2 112-122 DiseaseOrPhenotypicFeature denotes ichthyosis 0019269
T3 132-146 DiseaseOrPhenotypicFeature denotes (KID) syndrome 0018781
T4 160-169 DiseaseOrPhenotypicFeature denotes Keratitis 0003085
T5 170-180 DiseaseOrPhenotypicFeature denotes ichthyosis 0019269
T6 190-204 DiseaseOrPhenotypicFeature denotes (KID) syndrome 0018781
T7 210-214 DiseaseOrPhenotypicFeature denotes rare 0021136
T8 215-225 DiseaseOrPhenotypicFeature denotes congenital 0021140
T9 611-623 DiseaseOrPhenotypicFeature denotes KID syndrome 0018781
T10 923-931 DiseaseOrPhenotypicFeature denotes alopecia 0004907
T11 1068-1080 DiseaseOrPhenotypicFeature denotes KID syndrome 0018781
T12 1105-1119 DiseaseOrPhenotypicFeature denotes papillomatosis 0021098
T13 1329-1342 DiseaseOrPhenotypicFeature denotes hydrocephalus 0001150
T14 1401-1411 DiseaseOrPhenotypicFeature denotes meningitis 0021108
T15 1480-1501 DiseaseOrPhenotypicFeature denotes Klebsiella pneumoniae 0030602
T16 1510-1529 DiseaseOrPhenotypicFeature denotes respiratory failure 0021113
T17 1936-1948 DiseaseOrPhenotypicFeature denotes KID syndrome 0018781