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http://purl.uniprot.org/diseases/4189http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/4189http://www.w3.org/2000/01/rdf-schema#comment"A form of cone-rod dystrophy, an inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa, due to cone photoreceptors degenerating at a higher rate than rod photoreceptors."xsd:string
http://purl.uniprot.org/diseases/4189http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/182
http://purl.uniprot.org/diseases/4189http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/615973
http://purl.uniprot.org/diseases/4189http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D058499
http://purl.uniprot.org/diseases/4189http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN219005
http://purl.uniprot.org/diseases/4189http://www.w3.org/2004/02/skos/core#prefLabel"Cone-rod dystrophy 20"xsd:string
http://purl.uniprot.org/diseases/4189http://purl.uniprot.org/core/mnemonic"CORD20"xsd:string
http://purl.uniprot.org/uniprot/Q8TC44#SIPCE948A8E24BA04E7http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/4189
http://purl.uniprot.org/annotation/VAR_071916http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/4189
http://purl.uniprot.org/annotation/VAR_071917http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/4189
http://purl.uniprot.org/uniprot/#_CA0532992D24DCE9_up.disease_DADB24735F669E0Ehttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/4189