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http://purl.uniprot.org/diseases/2490http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/2490http://www.w3.org/2000/01/rdf-schema#comment"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/2490http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/182
http://purl.uniprot.org/diseases/2490http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/612775
http://purl.uniprot.org/diseases/2490http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D058499
http://purl.uniprot.org/diseases/2490http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1423873
http://purl.uniprot.org/diseases/2490http://www.w3.org/2004/02/skos/core#prefLabel"Cone-rod dystrophy 9"xsd:string
http://purl.uniprot.org/diseases/2490http://purl.uniprot.org/core/mnemonic"CORD9"xsd:string
http://purl.uniprot.org/uniprot/Q13443#SIP95226F401CDF2237http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2490
http://purl.uniprot.org/uniprot/#_1040863DCA2F5E9A_up.disease_40D30715D2F54D15http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/2490