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DESCRIBE <http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E>
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http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E
http://www.w3.org/2000/01/rdf-schema#comment
"Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy."
xsd:string
http://purl.uniprot.org/uniprot/#_B94F4A01B5D798960E0A374A13AA47A827A325732EEA6B38034FBD3C30C259603565BA37033B7DDC7FF4AC749FA3E606
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E
http://purl.uniprot.org/uniprot/B4DGG5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E
http://purl.uniprot.org/uniprot/#_B4DGG5-mappedCitation-36430690
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BA0579E61F3B04C9891E1A2136089C428D17B787ED26A7224B97AEED7112B2B0123DF0160BBB68D02A2ED26A783A9F3E