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http://purl.uniprot.org/keywords/911http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/911http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/1060
http://purl.uniprot.org/keywords/911http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/911http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/keywords/911http://www.w3.org/2000/01/rdf-schema#comment"Protein which, if defective, causes desmin-related myopathy (DRM), a clinically and genetically heterogeneous group of muscular disorders defined morphologically by intrasarcoplasmic aggregates of desmin, usually accompanied by other protein aggregates. Both autosomal dominant and autosomal recessive inheritance have been reported. Approximately one-third of DRMs are thought to be caused by mutations in the desmin gene."xsd:string
http://purl.uniprot.org/keywords/911http://www.w3.org/2004/02/skos/core#prefLabel"Desmin-related myopathy"xsd:string
http://purl.uniprot.org/keywords/911http://purl.uniprot.org/core/categoryhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/diseases/1481http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/911
http://purl.uniprot.org/diseases/795http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/911
http://purl.uniprot.org/uniprot/Q9NZV5http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/911
http://purl.uniprot.org/uniprot/P17661http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/911
http://purl.uniprot.org/uniprot/O95425http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/911
http://purl.uniprot.org/keywords/1060http://www.w3.org/2004/02/skos/core#narrowerhttp://purl.uniprot.org/keywords/911