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DESCRIBE <http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77>
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http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77
http://www.w3.org/2000/01/rdf-schema#comment
"In conclusion our data established the first linkage association of a loss-of-function mutation in the SPATA7 gene with a typical retinitis pigmentosa (RP) phenotype and not with leber congenital amaurosis or early onset RP."
xsd:string
http://purl.uniprot.org/uniprot/#_74B522F6B3EFAD54D7BE5B501CC5C501B8709FD93E484C29ADA0F33812462E8E839E445E89B5E14F67E369E58D4EF698
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77
http://purl.uniprot.org/uniprot/V9HVY9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77
http://purl.uniprot.org/uniprot/#_V9HVY9-mappedCitation-22136677
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DB41B2D784C060C15B813698182BF0B1ABC84CF7B4082AF9E0ECC8ECB43A75714BA5C76F9AAE35B112E709BBDB204C77