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DESCRIBE <http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518>
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http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518
http://www.w3.org/2000/01/rdf-schema#comment
"These results provide the first direct evidence that a mutation [in GCAP1] linked to congenital blindness increases Ca2+ in the outer segment which may trigger the apoptotic process."
xsd:string
http://purl.uniprot.org/uniprot/#_1D7318A8E005778F421B394E73EECD8BBEDFFAADF85DD651E05B8C678F3545E544E6AC3349128B4EBDE51A41BD90DBCA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518
http://purl.uniprot.org/uniprot/P43081
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518
http://purl.uniprot.org/uniprot/#_P43081-mappedCitation-15240799
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/332E85FB7F5ED4491EE269ED9A89B257918FA8549C015BDD280824FE16C9B1D149927020B9403504A17B2848F9ACC518