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DESCRIBE <http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE>
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http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE
http://www.w3.org/2000/01/rdf-schema#comment
"The researchers found a single SCN5A mutation association with arrhythmia in a familial cohort with atrial fibrillation which suggests this variation in the SCN5A gene is not a significant cause of familial atrial fibrillation"
xsd:string
http://purl.uniprot.org/uniprot/#_2A5EA2E99BE114FF63EDA2553FA66C6A8D964CEE5BE552B83348845B6CC802FEA586431C1CAA8F6EBE77479D7C543C3D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE
http://purl.uniprot.org/uniprot/Q8WWN5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE
http://purl.uniprot.org/uniprot/#_Q8WWN5-mappedCitation-18088563
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/65698EAE2487AEDF134A464B11F7D50B321FB81D4AE35597B8B589DABFF3DAB37AEC211C0F69E767F69E39A2A6C90ACE