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DESCRIBE <http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9>
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http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9
http://www.w3.org/2000/01/rdf-schema#comment
"The present report confirms the wide clinical spectrum of Peters plus syndrome underlines the major clinical criteria of the syndrome and the major implication of B3GALTL gene in this condition."
xsd:string
http://purl.uniprot.org/uniprot/#_7852D4ABC3A9AF32734C6B65F4E47F92CC26AB5F30C78DD2AD7C289767FE1A77E943934BE1BA46A34BA73D9DB25B5795
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9
http://purl.uniprot.org/uniprot/Q6Y288
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9
http://purl.uniprot.org/uniprot/#_Q6Y288-mappedCitation-21067481
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1FFB1A6BBD7EA3CE17780BCF6B8212EDE11985AD94EB83256F89140EBD445CF91D4C70A071BBF7BB374C554EAD19D8F9