PubMed:17033686 JSONTXT 33 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue originalLabel
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T3 96-114 DiseaseOrPhenotypicFeature denotes mental retardation D008607
T4 116-143 DiseaseOrPhenotypicFeature denotes X-linked mental retardation D038901
T5 180-189 DiseaseOrPhenotypicFeature denotes syndromic D013577
T6 207-216 DiseaseOrPhenotypicFeature denotes syndromic D013577
T7 466-484 DiseaseOrPhenotypicFeature denotes mental retardation D008607
T8 486-488 DiseaseOrPhenotypicFeature denotes MR D008607
T9 491-505 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T10 515-523 DiseaseOrPhenotypicFeature denotes coloboma D003103
T11 525-537 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T12 561-579 DiseaseOrPhenotypicFeature denotes spastic paraplegia D010264
T13 672-679 DiseaseOrPhenotypicFeature denotes disease D004194
T14 815-843 DiseaseOrPhenotypicFeature denotes Lenz microphthalmia syndrome C537464
T15 1171-1178 DiseaseOrPhenotypicFeature denotes disease D004194
T16 1230-1265 DiseaseOrPhenotypicFeature denotes Hamel cerebropalatocardiac syndrome C537761
T17 1549-1563 DiseaseOrPhenotypicFeature denotes microphthalmia D008850