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DESCRIBE <http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07>
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http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07
http://www.w3.org/2000/01/rdf-schema#comment
"we report the absence of mutations in all studied genes in four families with phenotypes associating cataract mental retardation and microcephaly."
xsd:string
http://purl.uniprot.org/uniprot/#_7769E760B5027539D183E6F166147F97574546E781F7F74BB008A5329C16FF86F7321A746316DDB0923A4FCAC6FF0362
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07
http://purl.uniprot.org/uniprot/O75364
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07
http://purl.uniprot.org/uniprot/#_O75364-mappedCitation-22103961
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1904003CD7DF16F3F4906598BBF819AAF283B8FD745E77C9641B7B296242133CE1CA1F415826B135BB80F937F0A5BC07