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DESCRIBE <http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA>
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http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); the G2019S mutation in LRRK2 is the most common genetic determinant of Parkinson's disease identified so far"
xsd:string
http://purl.uniprot.org/uniprot/#_D661A5F6D49CCD4551999517F1E0BE3BD258935784FF167D5697BAEF5260E1AF3B94354E90922E0F31E1477170183434
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA
http://purl.uniprot.org/uniprot/A2VED2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA
http://purl.uniprot.org/uniprot/#_A2VED2-mappedCitation-16272257
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/10C71D2CCD986CECCF6A0D7DB7BA804F1570F6D54703BAF9221290EA424853E685AF9A2EE206AB8D5D56F26AC21F63DA