| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
63-90 |
DiseaseOrPhenotypicFeature |
denotes |
multiple pterygium syndrome |
0009926|0017415 |
| T3 |
116-144 |
DiseaseOrPhenotypicFeature |
denotes |
Multiple pterygium syndromes |
0009926|0017415 |
| T5 |
146-149 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
0019249 |
| T6 |
303-317 |
DiseaseOrPhenotypicFeature |
denotes |
arthrogryposis |
0008779 |
| T7 |
320-323 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
0019249 |
| T8 |
575-578 |
DiseaseOrPhenotypicFeature |
denotes |
can |
0012833 |
| T9 |
611-614 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
0019249 |
| T10 |
773-776 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
0019249 |
| T11 |
840-843 |
DiseaseOrPhenotypicFeature |
denotes |
MPS |
0019249 |
| T12 |
1136-1159 |
DiseaseOrPhenotypicFeature |
denotes |
fetal akinesia sequence |
0008824 |
| T13 |
1211-1232 |
DiseaseOrPhenotypicFeature |
denotes |
congenital myasthenia |
0018940 |
| T14 |
1347-1368 |
DiseaseOrPhenotypicFeature |
denotes |
congenital myasthenia |
0018940 |
| T15 |
1399-1402 |
DiseaseOrPhenotypicFeature |
denotes |
can |
0012833 |
