| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
| T13041 |
0-5 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T34458 |
110-115 |
OrganismTaxon |
denotes |
human |
|
| T1 |
116-137 |
DiseaseOrPhenotypicFeature |
denotes |
basal cell carcinomas |
D002280 |
| T2 |
151-172 |
DiseaseOrPhenotypicFeature |
denotes |
Basal cell carcinomas |
D002280 |
| T3 |
174-178 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
| T8266 |
202-207 |
OrganismTaxon |
denotes |
human |
|
| T4 |
208-214 |
DiseaseOrPhenotypicFeature |
denotes |
cancer |
D009369 |
| T5 |
291-306 |
DiseaseOrPhenotypicFeature |
denotes |
Gorlin syndrome |
D001478 |
| T6 |
385-389 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
| T7 |
400-413 |
DiseaseOrPhenotypicFeature |
denotes |
birth defects |
D000013 |
| T8 |
443-447 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
| T9 |
485-490 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
D009369 |
| T23552 |
491-501 |
GeneOrGeneProduct |
denotes |
suppressor |
|
| T18452 |
507-512 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T26171 |
572-577 |
GeneOrGeneProduct |
denotes |
PTCH2 |
|
| T10 |
619-638 |
DiseaseOrPhenotypicFeature |
denotes |
genomic instability |
D042822 |
| T11 |
665-669 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
| T12 |
713-718 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
D009369 |
| T1490 |
792-797 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T60208 |
802-807 |
GeneOrGeneProduct |
denotes |
PTCH2 |
|
| T13 |
987-991 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
| T81502 |
1066-1075 |
SequenceVariant |
denotes |
g.2885G>C |
|
| T26397 |
1090-1095 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T65288 |
1129-1136 |
SequenceVariant |
denotes |
p.R962T |
|
| T14 |
1207-1212 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
D009369 |
| T78663 |
1226-1233 |
OrganismTaxon |
denotes |
patient |
|
| T15 |
1239-1254 |
DiseaseOrPhenotypicFeature |
denotes |
Gorlin syndrome |
D001478 |
| T44901 |
1275-1284 |
SequenceVariant |
denotes |
g.2839T>G |
|
| T82813 |
1329-1339 |
SequenceVariant |
denotes |
p.E947stop |
|
| T16 |
1379-1384 |
DiseaseOrPhenotypicFeature |
denotes |
tumor |
D009369 |
| T13987 |
1410-1414 |
SequenceVariant |
denotes |
217T |
|
| T78291 |
1430-1435 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T49187 |
1472-1477 |
GeneOrGeneProduct |
denotes |
PTCH1 |
|
| T17 |
1575-1579 |
DiseaseOrPhenotypicFeature |
denotes |
BCCs |
D002280 |
