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DESCRIBE <http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB>
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http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB
http://www.w3.org/2000/01/rdf-schema#comment
"NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss."
xsd:string
http://purl.uniprot.org/uniprot/#_57A8C0727031A3CCE7F0F7FC5177048226155AFC81A2A78890FC99EBE73D3B15E16F631A5E3B3C65BACB059A8C410298
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB
http://purl.uniprot.org/uniprot/Q59EE8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB
http://purl.uniprot.org/uniprot/#_Q59EE8-mappedCitation-33326993
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/497C6D0F32B24A6040E1A6C042BD20AC1603EE401AEF247C02B787DE771B884ED60AD4B343070DB9C169E9BEC57FEAEB