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DESCRIBE <http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864>
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http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864
http://www.w3.org/2000/01/rdf-schema#comment
"loss-of-function mutations in genes encoding the cardiac L-type calcium channel to be associated with a familial sudden cardiac death syndrome in which a Brugada syndrome phenotype is combined with shorter-than-normal QT intervals"
xsd:string
http://purl.uniprot.org/uniprot/#_06A0DF59917E3B80BF98A49CE2CB18BD3659C192FE1DA71A1FC1083865AB57429906CB2FF60B257564287C6E5371CA66
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864
http://purl.uniprot.org/uniprot/Q5VVH1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864
http://purl.uniprot.org/uniprot/#_Q5VVH1-mappedCitation-17224476
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6C820569DFD9576E14B17B393D35BE44FB6A08639416D426E54960F44D5E884B64A424CBDFB8BBB8D5C361F2D03A7864