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http://purl.uniprot.org/diseases/6596http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/6596http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive 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/6596http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/182
http://purl.uniprot.org/diseases/6596http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/613428
http://purl.uniprot.org/diseases/6596http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D000071700
http://purl.uniprot.org/diseases/6596http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3150691
http://purl.uniprot.org/diseases/6596http://www.w3.org/2004/02/skos/core#prefLabel"Cone-rod dystrophy 23"xsd:string
http://purl.uniprot.org/diseases/6596http://purl.uniprot.org/core/mnemonic"CORD23"xsd:string
http://purl.uniprot.org/uniprot/A6NGG8#SIP52AF08CC5C49D011http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/6596
http://purl.uniprot.org/uniprot/#_C6EC79810DCB3A41_up.disease_B893467E77DBAD6Bhttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/6596