PubMed:19101703 JSONTXT 26 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue mondo_id
T1 33-67 DiseaseOrPhenotypicFeature denotes oculopharyngeal muscular dystrophy 0008116
T2 81-115 DiseaseOrPhenotypicFeature denotes Oculopharyngeal muscular dystrophy 0008116
T3 117-121 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T4 175-179 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T5 410-414 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T6 516-520 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T7 641-645 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T8 766-769 DiseaseOrPhenotypicFeature denotes GCG 0008538
T9 772-775 DiseaseOrPhenotypicFeature denotes GCA 0008538
T10 807-810 DiseaseOrPhenotypicFeature denotes GCG 0008538
T11 813-816 DiseaseOrPhenotypicFeature denotes GCA 0008538
T12 818-821 DiseaseOrPhenotypicFeature denotes GCG 0008538
T13 824-827 DiseaseOrPhenotypicFeature denotes GCA 0008538
T14 857-860 DiseaseOrPhenotypicFeature denotes GCG 0008538
T15 906-910 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T16 958-961 DiseaseOrPhenotypicFeature denotes GCG 0008538
T17 983-987 DiseaseOrPhenotypicFeature denotes OPMD 0008116
T18 1033-1036 DiseaseOrPhenotypicFeature denotes GCG 0008538
T19 1088-1092 DiseaseOrPhenotypicFeature denotes OPMD 0008116