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DESCRIBE <http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D>
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http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); investigated whether the allelic variants 1019C and 1019T are differentially predictive of increased risk for coronary artery disease (CAD) and myocardial infarction (MI)"
xsd:string
http://purl.uniprot.org/uniprot/#_7406E44AE68C3ED9CD863A843B2765E03DA76571E18026D8307FAF574AABC36718396F2D1C382EBE33862566C6BC5E90
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D
http://purl.uniprot.org/uniprot/P35212
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D
http://purl.uniprot.org/uniprot/#_P35212-mappedCitation-16677656
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/52DDAF17F1E8E2E2268B84D3FFA572A08AA0407B9F6F726ADD7EFCA643C1DF4C79CE0C2BA014888CD06045603DF9267D