PubMed:17033686 JSONTXT 33 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label
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 193-197 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T6 227-231 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T7 363-367 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T8 382-386 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T9 444-484 DiseaseOrPhenotypicFeature denotes X-linked phenotype of mental retardation DISEASE
T10 486-488 DiseaseOrPhenotypicFeature denotes MR D008607
T11 491-505 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T12 515-523 DiseaseOrPhenotypicFeature denotes coloboma D003103
T13 525-537 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T14 539-555 DiseaseOrPhenotypicFeature denotes renal hypoplasia DISEASE
T15 561-579 DiseaseOrPhenotypicFeature denotes spastic paraplegia D010264
T16 815-843 DiseaseOrPhenotypicFeature denotes Lenz microphthalmia syndrome C537464
T17 1230-1265 DiseaseOrPhenotypicFeature denotes Hamel cerebropalatocardiac syndrome C537761
T18 1285-1289 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T19 1524-1528 DiseaseOrPhenotypicFeature denotes XLMR DISEASE
T20 1549-1563 DiseaseOrPhenotypicFeature denotes microphthalmia D008850