PubMed:22453924 / 0-169
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 |
T2 | 149-159 | gene:1756 | denotes | dystrophin |
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 |