PubMed:15958417 / 108-319
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T2 | 0-100 | Sentence | denotes | The Large(myd) mouse has a loss-of-function mutation in the putative glycosyltransferase gene Large. |
| TextSentencer_T3 | 101-211 | Sentence | denotes | Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D). |
| T2 | 0-211 | Sentence | denotes | The Large(myd) mouse has a loss-of-function mutation in the putative glycosyltransferase gene Large. Mutations in the human homolog (LARGE) have been described in a form of congenital muscular dystrophy (MDC1D). |
| T2 | 0-100 | Sentence | denotes | The Large(myd) mouse has a loss-of-function mutation in the putative glycosyltransferase gene Large. |
| T3 | 101-211 | 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 | 133-138 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | LARGE |
| _T11 | 173-202 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | denotes | congenital muscular dystrophy |
| _T12 | 173-209 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | congenital muscular dystrophy (MDC1D |
| _T13 | 204-209 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | MDC1D |
ICD10
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 184-202 | http://purl.bioontology.org/ontology/ICD10/G71.0 | denotes | muscular dystrophy |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 133-138 | http://www.uniprot.org/uniprot/Q9UH22 | denotes | LARGE |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 173-202 | Phenotype | denotes | congenital muscular dystrophy | HP:0003560 |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 173-202 | Disease | denotes | congenital muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0019950 |
| T3 | 204-209 | Disease | denotes | MDC1D | http://purl.obolibrary.org/obo/MONDO_0012138 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 15-20 | OrganismTaxon | denotes | mouse | 10088|10090 |
| T3 | 118-123 | OrganismTaxon | denotes | human | 9606 |