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DESCRIBE <http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D>
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http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D
http://www.w3.org/2000/01/rdf-schema#comment
"WDR19 mutations can cause a broad spectrum of ciliopathies that extends to Jeune and Sensenbrenner syndromes RP and renal NPHP-like phenotypes"
xsd:string
http://purl.uniprot.org/uniprot/#_8308171B923A391DF8005512C622F71ECBA638EB5F087152D948396052BFAFB128A1FCCF3588421B3624958721E7D8E8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D
http://purl.uniprot.org/uniprot/D6R9P6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D
http://purl.uniprot.org/uniprot/#_D6R9P6-mappedCitation-24504730
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/538D560158550DE0F9913B40B8371DDAA0851EFC6F271B890360A820A6CA9E777AB918AC8F6D9442F5FA59267252901D