| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
0-17 |
DiseaseOrPhenotypicFeature |
denotes |
Cockayne syndrome |
0016006 |
| T2 |
22-43 |
DiseaseOrPhenotypicFeature |
denotes |
xeroderma pigmentosum |
0019600 |
| T3 |
87-104 |
DiseaseOrPhenotypicFeature |
denotes |
Cockayne syndrome |
0016006 |
| T4 |
106-108 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T6 |
114-135 |
DiseaseOrPhenotypicFeature |
denotes |
xeroderma pigmentosum |
0019600 |
| T7 |
137-139 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T8 |
162-185 |
DiseaseOrPhenotypicFeature |
denotes |
disorders of DNA repair |
0021190 |
| T9 |
262-283 |
DiseaseOrPhenotypicFeature |
denotes |
xeroderma pigmentosum |
0019600 |
| T10 |
284-301 |
DiseaseOrPhenotypicFeature |
denotes |
Cockayne syndrome |
0016006 |
| T11 |
303-305 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T12 |
306-308 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T14 |
435-437 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T16 |
439-441 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T17 |
442-460 |
DiseaseOrPhenotypicFeature |
denotes |
neurologic disease |
0005071 |
| T19 |
470-472 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T18 |
470-483 |
DiseaseOrPhenotypicFeature |
denotes |
XP-CS complex |
0016354 |
| T20 |
473-475 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0016006 |
| T21 |
519-521 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T22 |
522-524 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T24 |
549-551 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T26 |
722-736 |
DiseaseOrPhenotypicFeature |
denotes |
leukodystrophy |
0019046 |
| T27 |
755-765 |
DiseaseOrPhenotypicFeature |
denotes |
neuropathy |
0005244 |
| T28 |
797-799 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T29 |
820-836 |
DiseaseOrPhenotypicFeature |
denotes |
photosensitivity |
0007559 |
| T30 |
844-848 |
DiseaseOrPhenotypicFeature |
denotes |
skin |
0002531 |
| T31 |
918-942 |
DiseaseOrPhenotypicFeature |
denotes |
squamous cell carcinomas |
0005096 |
| T32 |
981-1005 |
DiseaseOrPhenotypicFeature |
denotes |
nervous system neoplasms |
0021248 |
| T33 |
1033-1035 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T34 |
1220-1237 |
DiseaseOrPhenotypicFeature |
denotes |
axonal neuropathy |
0004183 |
| T35 |
1273-1275 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T37 |
1279-1281 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T38 |
1286-1300 |
DiseaseOrPhenotypicFeature |
denotes |
hypersensitive |
0000605 |
| T39 |
1348-1350 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T41 |
1360-1362 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T42 |
1460-1462 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T43 |
1553-1555 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T45 |
1569-1571 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T47 |
1591-1593 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T46 |
1591-1604 |
DiseaseOrPhenotypicFeature |
denotes |
XP-CS complex |
0016354 |
| T48 |
1594-1596 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0016006 |
| T49 |
1621-1623 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T50 |
1662-1664 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T52 |
1708-1710 |
DiseaseOrPhenotypicFeature |
denotes |
XP |
0019600 |
| T51 |
1708-1721 |
DiseaseOrPhenotypicFeature |
denotes |
XP-CS complex |
0016354 |
| T53 |
1711-1713 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0016006 |
| T54 |
1832-1834 |
DiseaseOrPhenotypicFeature |
denotes |
CS |
0008021|0016006 |
| T56 |
1855-1859 |
DiseaseOrPhenotypicFeature |
denotes |
skin |
0002531 |
| T57 |
1888-1899 |
DiseaseOrPhenotypicFeature |
denotes |
sensitivity |
0000605 |
| T58 |
2234-2245 |
DiseaseOrPhenotypicFeature |
denotes |
sensitivity |
0000605 |
| T59 |
2250-2270 |
DiseaseOrPhenotypicFeature |
denotes |
deficient DNA repair |
0021190 |
| T60 |
2359-2374 |
DiseaseOrPhenotypicFeature |
denotes |
premature aging |
0019303 |
