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DESCRIBE <http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E>
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http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E
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/#_E6F30D424C518EA4CC4C76EAE01988B8EB7B8755DCE5B4B0A9D87EAA58AA24E76B23469BB1D9837D29A884082342F5F9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E
http://purl.uniprot.org/uniprot/Q4VAQ0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E
http://purl.uniprot.org/uniprot/#_Q4VAQ0-mappedCitation-18464802
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5509193186D41DDF7473488A9CDF63DED25A487CBED0A2CF9BBFF3F2285675D6FAC7BA58F5F202B1843C9C5DA45AB44E