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PubMed:15987957 / 126-160 JSONTXT

Annnotations TAB JSON ListView MergeView

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T17 0-34 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 denotes hereditary inclusion body myopathy

ICD10

Id Subject Object Predicate Lexical cue
T1 26-34 http://purl.bioontology.org/ontology/ICD10/G72.9 denotes myopathy

GO-CC

Id Subject Object Predicate Lexical cue
T8 11-25 http://purl.obolibrary.org/obo/GO_0016234 denotes inclusion body

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 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
T1 26-34 Phenotype denotes myopathy HP:0003198