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PubMed:15033202 JSONTXT 25 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue mondo_id
T1 0-26 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T2 77-89 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T3 95-121 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T4 127-131 DiseaseOrPhenotypicFeature denotes rare 0021136
T5 228-238 DiseaseOrPhenotypicFeature denotes congenital 0021140
T6 239-251 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T7 360-386 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T8 516-528 DiseaseOrPhenotypicFeature denotes Microcephaly 0001149
T9 552-578 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T10 656-682 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T11 711-723 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T12 893-905 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T13 979-1005 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T14 1101-1127 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T15 1353-1379 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T16 1394-1420 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T17 1575-1601 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T18 1748-1774 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623
T19 1925-1951 DiseaseOrPhenotypicFeature denotes Nijmegen breakage syndrome 0009623