| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
54-70 |
DiseaseOrPhenotypicFeature |
denotes |
nephronophthisis |
0019005 |
| T2 |
113-129 |
DiseaseOrPhenotypicFeature |
denotes |
Nephronophthisis |
0019005 |
| T3 |
140-144 |
DiseaseOrPhenotypicFeature |
denotes |
rare |
0021136 |
| T4 |
155-176 |
DiseaseOrPhenotypicFeature |
denotes |
cystic kidney disease |
0002473 |
| T5 |
162-176 |
DiseaseOrPhenotypicFeature |
denotes |
kidney disease |
0005240 |
| T6 |
352-372 |
DiseaseOrPhenotypicFeature |
denotes |
retinal degeneration |
0004580 |
| T7 |
374-395 |
DiseaseOrPhenotypicFeature |
denotes |
Senior-Løken syndrome |
0017842 |
| T8 |
434-450 |
DiseaseOrPhenotypicFeature |
denotes |
Joubert syndrome |
0018772 |
| T9 |
780-790 |
DiseaseOrPhenotypicFeature |
denotes |
parametric |
0006887 |
| T10 |
1211-1233 |
DiseaseOrPhenotypicFeature |
denotes |
3 and Joubert syndrome |
0012078 |
| T11 |
1217-1233 |
DiseaseOrPhenotypicFeature |
denotes |
Joubert syndrome |
0018772 |
| T12 |
1732-1742 |
DiseaseOrPhenotypicFeature |
denotes |
congenital |
0021140 |
