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DESCRIBE <http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD>
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http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD
http://www.w3.org/2000/01/rdf-schema#comment
"The cone dystrophy associated with POC1B variants has features similar to achromatopsia and genetic analyses is useful in discriminating these two diseases."
xsd:string
http://purl.uniprot.org/uniprot/#_AFC3E69D90999563CED3931CF72905550F6C713F722E4165F166D4F72643DE1B567B881900624677C1DC3ACFBD402661
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD
http://purl.uniprot.org/uniprot/A0MNP0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD
http://purl.uniprot.org/uniprot/#_A0MNP0-mappedCitation-29220607
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4C65C3A7427C91767ACDB91268BE6316D49117661914C497C975A43FC4ABB156A6E24D7CB7FF9E3048DBDDC3E4D7ECDD