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DESCRIBE <http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE>
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http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE
http://www.w3.org/2000/01/rdf-schema#comment
"Compound heterozygous mutations in ABCG5 or ABCG8 causing Chinese familial Sitosterolemia."
xsd:string
http://purl.uniprot.org/uniprot/#_0FFE549DFA992A526E80618F5C6D2255A571F8062C81ECEAA767E36859DABA86BF32EB8AA4B3638D26DBFCBE82E66AC5
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE
http://purl.uniprot.org/uniprot/Q53T83
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE
http://purl.uniprot.org/uniprot/#_Q53T83-mappedCitation-32166861
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C00092C83DBC5EB5F404C1B45434C73A4F47C9276782649130489A87930F93BDE99FC38507B5474B2E3412111F495FAE