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DESCRIBE <http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483>
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http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483
http://www.w3.org/2000/01/rdf-schema#comment
"3 novel mutations have been identified in patients with the mitochondrial DNA depletion syndrome (c.1048G>A and c.1049G>T in SUCLA2 and c.531+4A>T in SUCLG1)."
xsd:string
http://purl.uniprot.org/uniprot/#_6D9726465A178758794FDA68881692F25D95839FF63B6E48055D8E14D172EAE70CB7E6D04B8651FDCEB43A78A8B67172
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483
http://purl.uniprot.org/uniprot/Q7Z503
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483
http://purl.uniprot.org/uniprot/#_Q7Z503-mappedCitation-22980518
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6D623A05F5F244AF73F3B2DE98525B3ECF8B446B393E1E9328827F696FD52E1B3862B1EF62F3C625DFFA885AE744C483