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DESCRIBE <http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30>
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http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30
http://www.w3.org/2000/01/rdf-schema#comment
"The SLC2A3 duplication was the most frequent CNV detected and the only significant finding in our combined analysis indicating that the SLC2A3 duplication might serve as a genetic modifier of congenital heart defect"
xsd:string
http://purl.uniprot.org/uniprot/#_19D3DB60C63FF4667EECC7D6F31A0C6F33868104B9405E6B0AEC8FA03EE29043839116A424E7083844314BA15185A7C6
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30
http://purl.uniprot.org/uniprot/P11169
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30
http://purl.uniprot.org/uniprot/#_P11169-mappedCitation-25892112
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0A0FC590CAC212893E5A92560FE7B9E57B2EF2BE0F89D9208A6A3A1989CA899B7C9A60F38F018C5EBB1EFE240842BC30