| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
60-70 |
DiseaseOrPhenotypicFeature |
denotes |
congenital |
0021140 |
| T2 |
79-93 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
0005420 |
| T4 |
186-196 |
DiseaseOrPhenotypicFeature |
denotes |
congenital |
0021140 |
| T3 |
186-211 |
DiseaseOrPhenotypicFeature |
denotes |
congenital hypothyroidism |
0018612 |
| T5 |
197-211 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
0005420 |
| T6 |
444-454 |
DiseaseOrPhenotypicFeature |
denotes |
congenital |
0021140 |
| T7 |
463-477 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
0005420 |
| T8 |
515-521 |
DiseaseOrPhenotypicFeature |
denotes |
anemia |
0002280 |
| T9 |
819-829 |
DiseaseOrPhenotypicFeature |
denotes |
completely |
0700063 |
| T10 |
1665-1685 |
DiseaseOrPhenotypicFeature |
denotes |
pituitary deficiency |
0015127 |
| T11 |
1768-1782 |
DiseaseOrPhenotypicFeature |
denotes |
hypothyroidism |
0005420 |
| T12 |
1833-1839 |
DiseaseOrPhenotypicFeature |
denotes |
anemia |
0002280 |
