| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
0-45 |
DiseaseOrPhenotypicFeature |
denotes |
Maternal uniparental disomy for chromosome 14 |
0019915 |
| T2 |
106-151 |
DiseaseOrPhenotypicFeature |
denotes |
maternal uniparental disomy for chromosome 14 |
0019915 |
| T3 |
181-183 |
DiseaseOrPhenotypicFeature |
denotes |
he |
0017319 |
| T4 |
247-268 |
DiseaseOrPhenotypicFeature |
denotes |
Prader-Willi syndrome |
0008300 |
| T5 |
270-273 |
DiseaseOrPhenotypicFeature |
denotes |
PWS |
0008300 |
| T6 |
301-308 |
DiseaseOrPhenotypicFeature |
denotes |
obesity |
0011122 |
| T7 |
336-350 |
DiseaseOrPhenotypicFeature |
denotes |
cryptorchidism |
0009047 |
| T8 |
417-448 |
DiseaseOrPhenotypicFeature |
denotes |
intrauterine growth retardation |
0005030 |
| T9 |
547-549 |
DiseaseOrPhenotypicFeature |
denotes |
he |
0017319 |
| T10 |
667-669 |
DiseaseOrPhenotypicFeature |
denotes |
he |
0017319 |
| T11 |
857-874 |
DiseaseOrPhenotypicFeature |
denotes |
sleep disturbance |
0100081 |
| T12 |
934-955 |
DiseaseOrPhenotypicFeature |
denotes |
Prader-Willi syndrome |
0008300 |
| T13 |
997-999 |
DiseaseOrPhenotypicFeature |
denotes |
he |
0017319 |
| T14 |
1059-1062 |
DiseaseOrPhenotypicFeature |
denotes |
PWS |
0008300 |
| T15 |
1125-1143 |
DiseaseOrPhenotypicFeature |
denotes |
precocious puberty |
0000088 |
| T16 |
1574-1577 |
DiseaseOrPhenotypicFeature |
denotes |
PWS |
0008300 |
