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DESCRIBE <http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E>
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http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E
http://www.w3.org/2000/01/rdf-schema#comment
"Study identified 21 patients with clinical features of Leigh syndrome who are either homozygous or compound heterozygous for SURF1 mutations."
xsd:string
http://purl.uniprot.org/uniprot/#_C198C5EDDB5394737E53E65A3D9DCDE1B33BCF621B6862C16882FC4C5F0457BF99E7F7D68A5AE374A9B9D0D522627B15
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E
http://purl.uniprot.org/uniprot/E5KRX5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E
http://purl.uniprot.org/uniprot/#_E5KRX5-mappedCitation-22488715
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/83D02DE4C103705146F33DFB57488B63DA1EE1CC041305C2EB322E94EBA15FB7CB261AE68BAB1FD4F40A0D0282C7972E