Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
T1 |
18-40 |
DiseaseOrPhenotypicFeature |
denotes |
cardiovascular disease |
0004995 |
T2 |
61-78 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
0005015 |
T3 |
141-158 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
0005015 |
T4 |
160-162 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T6 |
185-187 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T7 |
227-249 |
DiseaseOrPhenotypicFeature |
denotes |
cardiovascular disease |
0004995 |
T8 |
286-288 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T9 |
449-451 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T10 |
456-458 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T12 |
511-513 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T13 |
526-528 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T15 |
615-617 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T16 |
682-688 |
DiseaseOrPhenotypicFeature |
denotes |
stroke |
0005098 |
T17 |
690-711 |
DiseaseOrPhenotypicFeature |
denotes |
myocardial infarction |
0005068 |
T18 |
974-976 |
DiseaseOrPhenotypicFeature |
denotes |
CA |
0004992 |
T19 |
1100-1102 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T20 |
1107-1109 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T22 |
1249-1251 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T23 |
1320-1322 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T24 |
1336-1338 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T26 |
1379-1381 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T27 |
1415-1433 |
DiseaseOrPhenotypicFeature |
denotes |
myocardial infarct |
0005068 |
T28 |
1435-1441 |
DiseaseOrPhenotypicFeature |
denotes |
stroke |
0005098 |
T29 |
1507-1509 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T30 |
1514-1516 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T32 |
1655-1657 |
DiseaseOrPhenotypicFeature |
denotes |
DM |
0016367|0005015 |
T34 |
1678-1680 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |
T35 |
1714-1716 |
DiseaseOrPhenotypicFeature |
denotes |
Hp |
0008185 |