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DESCRIBE <http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74>
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http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74
http://www.w3.org/2000/01/rdf-schema#comment
"Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60 (HSPD1)"
xsd:string
http://purl.uniprot.org/uniprot/#_25D4D210B3C93557E587D58618C81C773ACE92EE0D984CC0C91994456CB868054629315C59EAA79C3EFA4D53B76C5B2A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74
http://purl.uniprot.org/uniprot/A0A0S2Z477
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74
http://purl.uniprot.org/uniprot/#_A0A0S2Z477-mappedCitation-11898127
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8D7A703E2AC4F326574BACAB0D4727E10B2AE8B8946334FFF0705D9FB0C8A018DAC9452C4743FB2BF0F70BFA5BAB3D74