PubMed:15958417 / 209-319
Annnotations
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T3 | 0-110 | Sentence | denotes | Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D). |
T3 | 0-110 | Sentence | denotes | Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D). |
GlycoBiology-GDGDB
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T2 | 32-37 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | LARGE |
_T11 | 72-101 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | denotes | congenital muscular dystrophy |
_T12 | 72-108 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | congenital muscular dystrophy (MDC1D |
_T13 | 103-108 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | MDC1D |
ICD10
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 83-101 | http://purl.bioontology.org/ontology/ICD10/G71.0 | denotes | muscular dystrophy |
uniprot-human
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T2 | 32-37 | http://www.uniprot.org/uniprot/Q9UH22 | denotes | LARGE |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 72-101 | Phenotype | denotes | congenital muscular dystrophy | HP:0003560 |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T2 | 72-101 | Disease | denotes | congenital muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0019950 |
T3 | 103-108 | Disease | denotes | MDC1D | http://purl.obolibrary.org/obo/MONDO_0012138 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T3 | 17-22 | OrganismTaxon | denotes | human | 9606 |