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DESCRIBE <http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84>
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http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84
http://www.w3.org/2000/01/rdf-schema#comment
"PLA2G6 mutations cause motor dysfunction phenotypes of young-onset dystonia-parkinsonism type 14 and can be relieved by DHA treatment in animal models."
xsd:string
http://purl.uniprot.org/uniprot/#_57E1F01BF40EF709D3DAF0C3CB09154A460A39773E3E6335BFBB255329BF3346A078B6D9EBB6F91F69ECCCCEB81A6218
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84
http://purl.uniprot.org/uniprot/P97819
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84
http://purl.uniprot.org/uniprot/#_P97819-mappedCitation-34520727
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EDA88BFE1108C1AFF6C3C52C6A55BF833341F3DC09FBC5D26491F868AC8A4764D1BA53C58FCBCE8921A06A672BDC0D84