PubMed:22453924 / 132-309
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T2 | 0-177 | Sentence | denotes | Mutations in the dystrophin gene without disruption of the reading frame often lead to Becker muscular dystrophy, but a genotype/phenotype correlation is difficult to establish. |
| T2 | 0-177 | Sentence | denotes | Mutations in the dystrophin gene without disruption of the reading frame often lead to Becker muscular dystrophy, but a genotype/phenotype correlation is difficult to establish. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 17-27 | gene:1756 | denotes | dystrophin |
| T3 | 87-112 | disease:C0917713 | denotes | Becker muscular dystrophy |
| R2 | T2 | T3 | associated_with | dystrophin,Becker muscular dystrophy |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 94-112 | HP_0003560 | denotes | muscular dystrophy |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 94-112 | HP:0003560 | denotes | muscular dystrophy |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 87-112 | ORDO:98895 | denotes | Becker muscular dystrophy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 87-112 | Disease | denotes | Becker muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0010311 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T2 | 94-112 | Phenotype | denotes | muscular dystrophy | HP:0003560 |