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DESCRIBE <http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1>
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http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1
http://www.w3.org/2000/01/rdf-schema#comment
"A point mutation in MYORG is associated with primary familial brain calcification in a Turkish family."
xsd:string
http://purl.uniprot.org/uniprot/#_4B23A20CA7C3BE62BB0670A5427A93F31351765C411763C147F0C42BA0A77B9A8D1AA35E540C7299F0F19B25B850D403
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1
http://purl.uniprot.org/uniprot/Q6NSJ0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1
http://purl.uniprot.org/uniprot/#_Q6NSJ0-mappedCitation-30649222
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FBE4EB633BD9DC4E84D0D998957B77A2853443AA7D8F60193D917CEF169904AC21871388B76912F846BA86E397DA4EC1