PubMed:22453924 / 0-131
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-131 | Sentence | denotes | Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy. |
| T1 | 0-131 | Sentence | denotes | Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 44-54 | gene:1756 | denotes | dystrophin |
| T1 | 105-130 | disease:C0917713 | denotes | Becker muscular dystrophy |
| R1 | T0 | T1 | associated_with | dystrophin,Becker muscular dystrophy |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 22453924-0#44#54#gene1756 | 44-54 | gene1756 | denotes | dystrophin |
| 22453924-0#105#130#diseaseC0917713 | 105-130 | diseaseC0917713 | denotes | Becker muscular dystrophy |
| 44#54#gene1756105#130#diseaseC0917713 | 22453924-0#44#54#gene1756 | 22453924-0#105#130#diseaseC0917713 | associated_with | dystrophin,Becker muscular dystrophy |
UBERON-AE
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T1 | 55-62 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 112-130 | HP:0003560 | denotes | muscular dystrophy |
performance-test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-UBERON-AE-B_T2 | 55-62 | http://purl.obolibrary.org/obo/UBERON_0012131 | denotes | central |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 105-130 | ORDO:98895 | denotes | Becker muscular dystrophy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 105-130 | Disease | denotes | Becker muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0010311 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 112-130 | Phenotype | denotes | muscular dystrophy | HP:0003560 |