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DESCRIBE <http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF>
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http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF
http://www.w3.org/2000/01/rdf-schema#comment
"SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot."
xsd:string
http://purl.uniprot.org/uniprot/#_66EAE054DB44E89970D00477EB887610E2B56E750B82D83D593C2EB251D41F0E3591B435DEE15CA22CC718AB5DFEDC38
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF
http://purl.uniprot.org/uniprot/Q9Y5X2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF
http://purl.uniprot.org/uniprot/#_Q9Y5X2-mappedCitation-24311514
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9413CE71CE80D5739C38C80F7A9BBA88DF9E659404A3AF2F1EBEF9B225D344CD8BE57F3FD80F6E6FFC1578AD8ACF20DF