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DESCRIBE <http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB>
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http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB
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/#_19E211A8B2AEC201F5CC87F45F8CE81724CD7ED25AEF1034E04B367F9D50725C54CC24E96359D67CFC7E3ACD6EAA12E4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB
http://purl.uniprot.org/uniprot/C9JFZ1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB
http://purl.uniprot.org/uniprot/#_C9JFZ1-mappedCitation-23804563
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/87C04328A1ED31A3E1E4FA941AF1644384F70AF5F19D9FA236B9DB82EF835E3948E5E8DA9CF7D70CA237D673D83E26BB