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DESCRIBE <http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A>
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http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in PDE6A and PDE6B accounted for 1.6% and 2.4% respectively in a cohort of French patients with rod-cone dystrophy (RCD)"
xsd:string
http://purl.uniprot.org/uniprot/#_2DD816212B0A47D7B9A5AA433991B02B23A00113C017E0E54BA5B92778E74553FB2C8D7E9C78DE36964371A9E3FA5FEA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A
http://purl.uniprot.org/uniprot/O75316
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A
http://purl.uniprot.org/uniprot/#_O75316-mappedCitation-30998820
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/02B2868578073679B12CC09AB5101A0C115B3073B6C835965EF94F635DF518337E71E621BEBAE14F1DE412F26088B43A