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DESCRIBE <http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4>
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http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4
http://www.w3.org/2000/01/rdf-schema#comment
"Identification of a novel triple heterozygous mutations in FA2H gene (c.968C>A; c.976G>A; c.688G>A) in a Chinese family with Hereditary Spastic Paraplegia Type 35."
xsd:string
http://purl.uniprot.org/uniprot/#_D5B38A4A066E5BA8265AEB93BAA44030B88000465BE1F7925395338A901BE3CE555865847278F575862587293CCBA486
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4
http://purl.uniprot.org/uniprot/Q7L5A8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4
http://purl.uniprot.org/uniprot/#_Q7L5A8-mappedCitation-23566484
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/26AF5FEAAA34B8C5C4760EFCD1A793F0D5E9596C33E50B66C2CCD797DB1717F3CC9D875DBE8DD1ACC430A7EA13ECB3C4