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DESCRIBE <http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79>
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http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79
http://www.w3.org/2000/01/rdf-schema#comment
"This is the third reported family with autosomal recessive early-onset parkinsonism associated with the SYNJ1 p.Arg258Gln mutation. This work contributes to the definition of the genetic and clinical aspects of PARK20."
xsd:string
http://purl.uniprot.org/uniprot/#_6AFE762AA8A1FE4092C44DCD6FF380157E630285720877F5EC7DEA4A2B58838ADABB03F4527A2AC85BE4B8F5DDE069CA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79
http://purl.uniprot.org/uniprot/J3KQV8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79
http://purl.uniprot.org/uniprot/#_J3KQV8-mappedCitation-24816432
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/28C543345DFA064810172808C0E61D07BD3ED6F51D4E20DC24AA3D6644875466C7A55BE12EBAC35862B774ABF4F96C79