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http://purl.uniprot.org/diseases/1063http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive disorder characterized by childhood-onset of cerebellar ataxia and exercise intolerance. Patient manifest gait ataxia and cerebellar atrophy with slow progression. Additional features include brisk tendon reflexes and Hoffmann sign, variable psychomotor retardation and variable seizures."xsd:string
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/1274
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/523
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/612016
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D028361
http://purl.uniprot.org/diseases/1063http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C2677589
http://purl.uniprot.org/diseases/1063http://www.w3.org/2004/02/skos/core#prefLabel"Coenzyme Q10 deficiency, primary, 4"xsd:string
http://purl.uniprot.org/diseases/1063http://purl.uniprot.org/core/mnemonic"COQ10D4"xsd:string
http://purl.uniprot.org/diseases/1063http://www.w3.org/2004/02/skos/core#altLabel"ARCA2"xsd:string
http://purl.uniprot.org/diseases/1063http://www.w3.org/2004/02/skos/core#altLabel"Autosomal recessive cerebellar ataxia type 2"xsd:string
http://purl.uniprot.org/diseases/1063http://www.w3.org/2004/02/skos/core#altLabel"SCAR9"xsd:string
http://purl.uniprot.org/diseases/1063http://www.w3.org/2004/02/skos/core#altLabel"Spinocerebellar ataxia autosomal recessive 9"xsd:string
http://purl.uniprot.org/uniprot/Q8NI60#SIP77E0177A87BBFF6Chttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044402http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044403http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044404http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044405http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044406http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044407http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_044408http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_072622http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_072623http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_072624http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063
http://purl.uniprot.org/annotation/VAR_072625http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/1063