PubMed:15987957 / 0-215 JSONTXT

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{"project":"uniprot-mouse","denotations":[{"id":"T1","span":{"begin":79,"end":105},"obj":"http://www.uniprot.org/uniprot/Q91WG8"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

{"project":"GO-BP","denotations":[{"id":"T1","span":{"begin":79,"end":116},"obj":"http://purl.obolibrary.org/obo/GO_0009384"},{"id":"T2","span":{"begin":99,"end":116},"obj":"http://purl.obolibrary.org/obo/GO_0033674"},{"id":"T3","span":{"begin":99,"end":116},"obj":"http://purl.obolibrary.org/obo/GO_0016301"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

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{"project":"NGLY1-deficiency","denotations":[{"id":"PD-NGLY1-deficiency-B_T1","span":{"begin":43,"end":62},"obj":"chem:24139"}],"namespaces":[{"prefix":"hgnc","uri":"https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:"},{"prefix":"omim","uri":"https://www.omim.org/entry/"},{"prefix":"chem","uri":"https://pubchem.ncbi.nlm.nih.gov/compound/"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"15987957-1#0#34#diseaseC1853926","span":{"begin":162,"end":196},"obj":"diseaseC1853926"},{"id":"15987957-1#36#40#diseaseC1853926","span":{"begin":198,"end":202},"obj":"diseaseC1853926"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":126,"end":160},"obj":"Disease"},{"id":"T2","span":{"begin":162,"end":196},"obj":"Disease"},{"id":"T3","span":{"begin":198,"end":202},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0007827"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0007827"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0007827"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":152,"end":160},"obj":"Phenotype"},{"id":"T2","span":{"begin":188,"end":196},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0003198"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0003198"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}

{"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":120,"end":125},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"9606"}],"text":"Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.\nHereditary inclusion body myopathy (HIBM) is an autos"}