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DESCRIBE <http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566>
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http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566
http://www.w3.org/2000/01/rdf-schema#comment
"Our data suggest that the previously reported Arg258Gln mutation in SYNJ1 is not a frequent cause of Parkinson disease"
xsd:string
http://purl.uniprot.org/uniprot/#_C8FF2042A5DAA72C47DA68B037ABC4CE4C02CE91CDDCE049D57021474B35A076B343D028769BBD65FD2EC5C842C4C1D2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566
http://purl.uniprot.org/uniprot/Q05CZ1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566
http://purl.uniprot.org/uniprot/#_Q05CZ1-mappedCitation-24609975
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/71D69F8C8AC747652EE7B89E8F56D49A81F7FC382060DAE1688BE2940F9E187B1AEF5D34E7F6654CA89BC7E791880566