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DESCRIBE <http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3>
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http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3
http://www.w3.org/2000/01/rdf-schema#comment
"These results indicated that the 540C>A nonsense mutation in RHAG gene caused the regulator type of Rhnull phenotype in a Chinese individual."
xsd:string
http://purl.uniprot.org/uniprot/#_C37DC2FE56E67F9B31992C915436266EA032842AEE75B2024C55E815C3CB3C52DC004F24B253C150CBB355556F3DF0C3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3
http://purl.uniprot.org/uniprot/Q9UP76
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3
http://purl.uniprot.org/uniprot/#_Q9UP76-mappedCitation-28063760
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FCAAF1FF0C25F3544BF59969241B78A3555D57E2C1F7C56FBEE411E40F7FFFFE8ABC9E258194AAC07BDD598C026705D3