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DESCRIBE <http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69>
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http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69
http://www.w3.org/2000/01/rdf-schema#comment
"This study has shown loss of Mg(2+) efflux function consequent to SLC41A1 R244H variant and SLC41A1 coding variants seem to be rare in Taiwanese Parkinson disease."
xsd:string
http://purl.uniprot.org/uniprot/#_132DD72E06272033539E63AE8F30A67D5C9DF1A78C6A53B57B3E9EA44D600960B4F96A3B0BC14021ED583EA34C8023F5
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69
http://purl.uniprot.org/uniprot/Q8IVJ1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69
http://purl.uniprot.org/uniprot/#_Q8IVJ1-mappedCitation-24661466
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/25C83BDB79AEF985073C9583912A9CA433C515D35A07D309BE04FC8B5B392BA25141817AF119C6A4F75453A60FEF3A69