| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
4-6 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T2 |
93-97 |
DiseaseOrPhenotypicFeature |
denotes |
MCUL |
0007888 |
| T3 |
99-104 |
DiseaseOrPhenotypicFeature |
denotes |
HLRCC |
0007888 |
| T4 |
106-120 |
DiseaseOrPhenotypicFeature |
denotes |
tumor syndrome |
0021058 |
| T5 |
136-155 |
DiseaseOrPhenotypicFeature |
denotes |
fumarase deficiency |
0011730 |
| T6 |
217-219 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T7 |
403-405 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T8 |
475-484 |
DiseaseOrPhenotypicFeature |
denotes |
Leiomyoma |
0001572 |
| T9 |
542-544 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T10 |
562-603 |
DiseaseOrPhenotypicFeature |
denotes |
multiple cutaneous and uterine leiomyomas |
0007888 |
| T11 |
606-610 |
DiseaseOrPhenotypicFeature |
denotes |
MCUL |
0007888 |
| T12 |
643-660 |
DiseaseOrPhenotypicFeature |
denotes |
renal cell cancer |
0005549|0003007 |
| T14 |
733-780 |
DiseaseOrPhenotypicFeature |
denotes |
hereditary leiomyomatosis and renal cell cancer |
0007888 |
| T15 |
782-787 |
DiseaseOrPhenotypicFeature |
denotes |
HLRCC |
0007888 |
| T16 |
825-827 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T17 |
833-838 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
0005070 |
| T18 |
1092-1094 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T19 |
1444-1446 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T20 |
1655-1657 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T21 |
1723-1725 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T22 |
1764-1768 |
DiseaseOrPhenotypicFeature |
denotes |
MCUL |
0007888 |
| T23 |
2052-2054 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T24 |
2090-2092 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T25 |
2176-2178 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T26 |
2447-2449 |
DiseaseOrPhenotypicFeature |
denotes |
FH |
0016525 |
| T27 |
2475-2484 |
DiseaseOrPhenotypicFeature |
denotes |
syndromes |
0002254 |
