| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
| T73070 |
0-44 |
DiseaseOrPhenotypicFeature |
denotes |
Ectodermal dysplasia-skin fragility syndrome |
C536183 |
| T254 |
87-94 |
SequenceVariant |
denotes |
888delC |
|
| T1 |
122-135 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
|
| T3596 |
169-187 |
DiseaseOrPhenotypicFeature |
denotes |
inherited disorder |
DISEASE |
| T2 |
214-227 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
|
| T32858 |
242-286 |
DiseaseOrPhenotypicFeature |
denotes |
ectodermal dysplasia-skin fragility syndrome |
C536183 |
| T95371 |
365-379 |
DiseaseOrPhenotypicFeature |
denotes |
skin fragility |
DISEASE |
| T73192 |
393-412 |
DiseaseOrPhenotypicFeature |
denotes |
plantar keratoderma |
DISEASE |
| T11431 |
414-428 |
DiseaseOrPhenotypicFeature |
denotes |
nail dystrophy |
DISEASE |
| T98095 |
434-442 |
DiseaseOrPhenotypicFeature |
denotes |
alopecia |
D000505 |
| T3 |
444-448 |
GeneOrGeneProduct |
denotes |
Skin |
|
| T4 |
597-610 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
|
| T5 |
616-620 |
GeneOrGeneProduct |
denotes |
PKP1 |
|
| T20656 |
643-656 |
SequenceVariant |
denotes |
deletion of C |
|
| T6 |
721-725 |
GeneOrGeneProduct |
denotes |
PKP1 |
|
| T8 |
803-817 |
DiseaseOrPhenotypicFeature |
denotes |
genodermatosis |
DISEASE |
| T7 |
912-925 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
|
