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http://purl.uniprot.org/diseases/3355http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/3355http://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/3355http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/182
http://purl.uniprot.org/diseases/3355http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/614500
http://purl.uniprot.org/diseases/3355http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D000071700
http://purl.uniprot.org/diseases/3355http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3281045
http://purl.uniprot.org/diseases/3355http://www.w3.org/2004/02/skos/core#prefLabel"Cone-rod dystrophy 16"xsd:string
http://purl.uniprot.org/diseases/3355http://purl.uniprot.org/core/mnemonic"CORD16"xsd:string
http://purl.uniprot.org/diseases/3355http://www.w3.org/2004/02/skos/core#altLabel"Retinal dystrophy with early macular involvement"xsd:string
http://purl.uniprot.org/uniprot/Q96NL8#SIPCA1D5FD0747FE2C7http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/3355
http://purl.uniprot.org/annotation/VAR_067305http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3355
http://purl.uniprot.org/uniprot/#_35D43EFC85B5078E_up.disease_4890C30F7566F148http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/3355