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DESCRIBE <http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407>
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http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407
http://www.w3.org/2000/01/rdf-schema#comment
"Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12) whereas null alleles cause the majority of Usher syndrome (Usher 1D)."
xsd:string
http://purl.uniprot.org/uniprot/#_5999AC1DC5C0B1F407DF764AC080DD39169C8F6D07D090528F6C4FF7C7FE165E30A8817F1931C4AA24B5C0FB4F154B11
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407
http://purl.uniprot.org/uniprot/A5D6V9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407
http://purl.uniprot.org/uniprot/#_A5D6V9-mappedCitation-16550584
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FE02BBA52D2628B8AB5863D07B3AA4246CCBD28915E5EE74E877D8798D5DF1D49685D56FC1266369B4C0444AD2B35407