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DESCRIBE <http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68>
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http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68
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/#_F2E40A87EED956B1D0A753E0BD6AB0414AD5D217C667C6E36E68A92155740DC8C9E1B71FB4C1011A50178CC06F684B62
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68
http://purl.uniprot.org/uniprot/L8EAB0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68
http://purl.uniprot.org/uniprot/#_L8EAB0-mappedCitation-16550584
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DC214753C0832322DA483E8925CE8259EA73C699383DE10C8288734804BAB741A19CA8F99DCC373EE66058A6A9C51F68