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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D>
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http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D
http://www.w3.org/2000/01/rdf-schema#comment
"Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_1355FFA09289B65E42C042C522F810779E35A04327D785F188AC3C79453139CF9E10BE744402A9C8EF2F2066AFF5BA10
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D
http://purl.uniprot.org/uniprot/O60683
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D
http://purl.uniprot.org/uniprot/#_O60683-mappedCitation-14713216
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/BFD1C9C194BDBC71C2ACC08F5A0E2BF13CE37992DAFF31A578C2472D4D0D8107CBE53C39D7B69D5E23B296B53371081D