| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
74-88 |
DiseaseOrPhenotypicFeature |
denotes |
Apert syndrome |
0007041 |
| T2 |
90-106 |
DiseaseOrPhenotypicFeature |
denotes |
Craniosynostosis |
0015469 |
| T3 |
107-116 |
DiseaseOrPhenotypicFeature |
denotes |
syndromes |
0002254 |
| T4 |
146-163 |
DiseaseOrPhenotypicFeature |
denotes |
skeletal diseases |
0005381 |
| T5 |
251-265 |
DiseaseOrPhenotypicFeature |
denotes |
Apert syndrome |
0007041 |
| T6 |
297-313 |
DiseaseOrPhenotypicFeature |
denotes |
craniosynostosis |
0015469 |
| T7 |
314-323 |
DiseaseOrPhenotypicFeature |
denotes |
syndromes |
0002254 |
| T8 |
354-364 |
DiseaseOrPhenotypicFeature |
denotes |
syndactyly |
0019530|0021002 |
| T10 |
396-432 |
DiseaseOrPhenotypicFeature |
denotes |
central nervous system malformations |
0020022 |
| T11 |
1062-1072 |
DiseaseOrPhenotypicFeature |
denotes |
dependence |
0004938 |
