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http://purl.uniprot.org/diseases/5924http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive disorder characterized by severe, early lethal neurodegeneration, myasthenic and myopathic features, progressive cerebral atrophy with myelination defects, and intractable epilepsy."xsd:string
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/887
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/523
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/619036
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/991
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D065886
http://purl.uniprot.org/diseases/5924http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN292948
http://purl.uniprot.org/diseases/5924http://www.w3.org/2004/02/skos/core#prefLabel"Myopathy, epilepsy, and progressive cerebral atrophy"xsd:string
http://purl.uniprot.org/diseases/5924http://purl.uniprot.org/core/mnemonic"MEPCA"xsd:string
http://purl.uniprot.org/uniprot/Q96F25#SIPE876D0457EEC397Ahttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/5924
http://purl.uniprot.org/annotation/VAR_084707http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5924
http://purl.uniprot.org/annotation/VAR_084709http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5924
http://purl.uniprot.org/annotation/VAR_084710http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/5924
http://purl.uniprot.org/uniprot/#_03FFA5382E228960_up.disease_2E1CBA88B4822B98http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/5924