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DESCRIBE <http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37>
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http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37
http://www.w3.org/2000/01/rdf-schema#comment
"These data constitute the first report of a heterozygous Q455V mutation of the COL8A2 gene in Korean patients with Fuchs' corneal dystrophy and Q455V may be the causative defect in the development and progression of Korean FECD patients."
xsd:string
http://purl.uniprot.org/uniprot/#_14787AAD2F8063E76039638375A35702EBFF404044031C00D927E990A1A31B792CECCF7137A7A9A26A912B0F4E6BACFF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37
http://purl.uniprot.org/uniprot/P25067
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37
http://purl.uniprot.org/uniprot/#_P25067-mappedCitation-18464802
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9296751CDCA35E36C28B271FC069F6A2F5F35D4D1120568FFD99B4153439C7E989641627F911D8BEDD877778B4762C37