| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
62-76 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
| T2 |
78-90 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
0001149 |
| T3 |
96-114 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
0001071 |
| T4 |
125-143 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
0001071 |
| T5 |
224-226 |
DiseaseOrPhenotypicFeature |
denotes |
NS |
0009735 |
| T6 |
351-354 |
DiseaseOrPhenotypicFeature |
denotes |
can |
0012833 |
| T7 |
379-381 |
DiseaseOrPhenotypicFeature |
denotes |
NS |
0009735 |
| T8 |
466-484 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
0001071 |
| T9 |
486-488 |
DiseaseOrPhenotypicFeature |
denotes |
MR |
0001071 |
| T10 |
491-505 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
| T11 |
515-523 |
DiseaseOrPhenotypicFeature |
denotes |
coloboma |
0001476 |
| T12 |
525-537 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
0001149 |
| T13 |
539-555 |
DiseaseOrPhenotypicFeature |
denotes |
renal hypoplasia |
0019637 |
| T14 |
561-579 |
DiseaseOrPhenotypicFeature |
denotes |
spastic paraplegia |
0019064 |
| T15 |
815-843 |
DiseaseOrPhenotypicFeature |
denotes |
Lenz microphthalmia syndrome |
0010671 |
| T16 |
1230-1265 |
DiseaseOrPhenotypicFeature |
denotes |
Hamel cerebropalatocardiac syndrome |
0019767 |
| T17 |
1549-1563 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
