PubMed:15987957 / 162-196 JSONTXT

Annnotations TAB JSON ListView MergeView

    GlycoBiology-GDGDB

    {"project":"GlycoBiology-GDGDB","denotations":[{"id":"_T18","span":{"begin":0,"end":34},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385"}],"text":"Hereditary inclusion body myopathy"}

    ICD10

    {"project":"ICD10","denotations":[{"id":"T2","span":{"begin":26,"end":34},"obj":"http://purl.bioontology.org/ontology/ICD10/G72.9"}],"text":"Hereditary inclusion body myopathy"}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T9","span":{"begin":11,"end":25},"obj":"http://purl.obolibrary.org/obo/GO_0016234"}],"text":"Hereditary inclusion body myopathy"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"15987957-1#0#34#diseaseC1853926","span":{"begin":0,"end":34},"obj":"diseaseC1853926"}],"text":"Hereditary inclusion body myopathy"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T2","span":{"begin":0,"end":34},"obj":"Disease"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0007827"}],"text":"Hereditary inclusion body myopathy"}

    HP-phenotype

    {"project":"HP-phenotype","denotations":[{"id":"T2","span":{"begin":26,"end":34},"obj":"Phenotype"}],"attributes":[{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0003198"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Hereditary inclusion body myopathy"}