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DESCRIBE <http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63>
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http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63
http://www.w3.org/2000/01/rdf-schema#comment
"The results of this study confirm that HSJ1 mutations are a rare but detectable cause of autosomal recessive dHMN and CMT2."
xsd:string
http://purl.uniprot.org/uniprot/#_A9AB8BCB9127AF2CEEBD97181692A8B0012CB28C2523E57A162DD94C83D54D360E8953FB1C4FB3EA92BECCF810A44513
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63
http://purl.uniprot.org/uniprot/A8K0R1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63
http://purl.uniprot.org/uniprot/#_A8K0R1-mappedCitation-25274842
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D7D25502DA3C71BF03DAD84EBC0277D2AC3BC20B2E58B33060B2F923963293D6C06FDA09943B5F419D00A3BC8139FF63