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DESCRIBE <http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A>
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http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A
http://www.w3.org/2000/01/rdf-schema#comment
"The phenotype is best uniformly termed congenital cone-rod synaptic disorder. In Saudi Arabia a founder homozygous c.81_82insA CABP4 mutation is a recurrent cause."
xsd:string
http://purl.uniprot.org/uniprot/#_BBCBCCE2CEC7ED7E62D481470A238B86B8A1CE529A5BFFD97425E9512A774864B1D3B375609DFFE1A57FC8A37924A901
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A
http://purl.uniprot.org/uniprot/Q06546
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A
http://purl.uniprot.org/uniprot/#_Q06546-mappedCitation-23099293
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/966D376376F6A932D010441ABDCA05AB91412217CC582AB74B2C084BB4A725887BE96118FAE1606F16BAF08645A7621A