PubMed:15987957 / 162-196
Annnotations
GlycoBiology-GDGDB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T18 | 0-34 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | denotes | Hereditary inclusion body myopathy |
ICD10
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 26-34 | http://purl.bioontology.org/ontology/ICD10/G72.9 | denotes | myopathy |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T9 | 11-25 | http://purl.obolibrary.org/obo/GO_0016234 | denotes | inclusion body |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 15987957-1#0#34#diseaseC1853926 | 0-34 | diseaseC1853926 | denotes | Hereditary inclusion body myopathy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 0-34 | Disease | denotes | Hereditary inclusion body myopathy | http://purl.obolibrary.org/obo/MONDO_0007827 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T2 | 26-34 | Phenotype | denotes | myopathy | HP:0003198 |