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DESCRIBE <http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A>
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http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); mutations in the PCSK9 gene cause autosomal dominant hypercholesterolemia."
xsd:string
http://purl.uniprot.org/uniprot/#_9B0D09BCD7483EB8A524803572025C6774BDD3FD2096BD9CECE4726C0B1BB74C3745AA77C8B7AEDBC7BE7BE6E9849280
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A
http://purl.uniprot.org/uniprot/Q8NBP7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A
http://purl.uniprot.org/uniprot/#_Q8NBP7-mappedCitation-15099351
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CBC8A5F6BF8C4D0ADAF888F2D3718ED5E919773B49B462849EE13A34E9BD2C8A8EB49C3D9C308AC806C6E1C221F81D9A