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DESCRIBE <http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A>
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http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A
http://www.w3.org/2000/01/rdf-schema#comment
"Findings suggest that SYNJ1 mutation is responsible for the early-onset Parkinsonism phenotype probably due to deficiencies in its phosphatase activity and consequent impairment of its synaptic functions."
xsd:string
http://purl.uniprot.org/uniprot/#_49B7878AF0048AE8E20EF1C95503D801E441B22E719009750E36C4DEE5D4D8EA610D27B2C4E0417D24EC331F357C016C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A
http://purl.uniprot.org/uniprot/J3KQV8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A
http://purl.uniprot.org/uniprot/#_J3KQV8-mappedCitation-23804563
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/405E578575D0BAB533F40C6EDD4590F30BC871E87589D773125DDE489A42A5DB76A1113158069F16492F9B1B5FEE102A