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DESCRIBE <http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0>
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http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0
http://www.w3.org/2000/01/rdf-schema#comment
"An autosomal recessive juvenile parkinsonism patient had a homozygous exon 3 deletion in the parkin gene and [alpha]-synuclein-positive inclusions suggesting a close relationship between ARJP and idiopathic PD."
xsd:string
http://purl.uniprot.org/uniprot/#_D1E43DDBC67F49687C6A769430A9A8C341B3330D3EF9AE00E19A7FB25C407018DD61C3FA63DCB9F517FE105055BA6751
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0
http://purl.uniprot.org/uniprot/S4X465
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0
http://purl.uniprot.org/uniprot/#_S4X465-mappedCitation-15326242
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/88024074643789EC0DA9633A008842FE6308C58B9B6DD70BE83CA2EBD5013A1EA0136B04F8CAA8DB30A719B3907831D0