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http://purl.uniprot.org/diseases/3874http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive, mitochondrial disorder characterized by hypertrophic cardiomyopathy, liver steatosis, and decreased levels of mitochondrial complexes I and IV in heart and skeletal muscle."xsd:string
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/1274
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/615395
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D028361
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3809339
http://purl.uniprot.org/diseases/3874http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN179856
http://purl.uniprot.org/diseases/3874http://www.w3.org/2004/02/skos/core#prefLabel"Combined oxidative phosphorylation deficiency 16"xsd:string
http://purl.uniprot.org/diseases/3874http://purl.uniprot.org/core/mnemonic"COXPD16"xsd:string
http://purl.uniprot.org/uniprot/Q9H9J2#SIP1B493DF6CB6D632Fhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/3874
http://purl.uniprot.org/annotation/VAR_070568http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3874
http://purl.uniprot.org/uniprot/#_4B7A780883F47C02_up.disease_BAC0567721B492EChttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/3874