| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 3016 |
0-44 |
DiseaseOrPhenotypicFeature |
denotes |
Ectodermal dysplasia-skin fragility syndrome |
MESH:C536183 |
| 3017 |
87-94 |
SequenceVariant |
denotes |
888delC |
c|DEL888|C |
| 3018 |
122-135 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
NCBIGene:5317 |
| 3019 |
169-187 |
DiseaseOrPhenotypicFeature |
denotes |
inherited disorder |
MESH:D030342 |
| 3020 |
214-227 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
NCBIGene:5317 |
| 3021 |
242-286 |
DiseaseOrPhenotypicFeature |
denotes |
ectodermal dysplasia-skin fragility syndrome |
MESH:C536183 |
| 3022 |
365-379 |
DiseaseOrPhenotypicFeature |
denotes |
skin fragility |
MESH:C536183 |
| 3023 |
393-412 |
DiseaseOrPhenotypicFeature |
denotes |
plantar keratoderma |
MESH:D017499 |
| 3024 |
414-428 |
DiseaseOrPhenotypicFeature |
denotes |
nail dystrophy |
MESH:D009260 |
| 3025 |
434-442 |
DiseaseOrPhenotypicFeature |
denotes |
alopecia |
MESH:D000505 |
| 3026 |
597-610 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
NCBIGene:5317 |
| 3027 |
616-620 |
GeneOrGeneProduct |
denotes |
PKP1 |
NCBIGene:5317 |
| 3028 |
643-674 |
SequenceVariant |
denotes |
deletion of C at nucleotide 888 |
c|DEL888|C |
| 3029 |
721-725 |
GeneOrGeneProduct |
denotes |
PKP1 |
NCBIGene:5317 |
| 3030 |
803-817 |
DiseaseOrPhenotypicFeature |
denotes |
genodermatosis |
MESH:D012873 |
| 3031 |
912-925 |
GeneOrGeneProduct |
denotes |
plakophilin 1 |
NCBIGene:5317 |
