| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
0-7 |
DiseaseOrPhenotypicFeature |
denotes |
Hepatic |
0002251 |
| T2 |
65-83 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
0011426 |
| T3 |
133-151 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
0011426 |
| T4 |
157-161 |
DiseaseOrPhenotypicFeature |
denotes |
rare |
0021136 |
| T5 |
182-207 |
DiseaseOrPhenotypicFeature |
denotes |
neurodegenerative disease |
0005559 |
| T6 |
288-306 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
0005395 |
| T7 |
308-328 |
DiseaseOrPhenotypicFeature |
denotes |
retinal degeneration |
0004580 |
| T8 |
334-351 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
0005015 |
| T9 |
597-615 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
0011426 |
| T10 |
672-690 |
DiseaseOrPhenotypicFeature |
denotes |
movement disorders |
0005395 |
| T11 |
984-1002 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
0011426 |
| T12 |
1067-1074 |
DiseaseOrPhenotypicFeature |
denotes |
hepatic |
0002251 |
| T13 |
1181-1188 |
DiseaseOrPhenotypicFeature |
denotes |
Hepatic |
0002251 |
| T14 |
1470-1488 |
DiseaseOrPhenotypicFeature |
denotes |
Aceruloplasminemia |
0011426 |
| T15 |
1636-1654 |
DiseaseOrPhenotypicFeature |
denotes |
aceruloplasminemia |
0011426 |
| T16 |
1836-1843 |
DiseaseOrPhenotypicFeature |
denotes |
hepatic |
0002251 |
