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DESCRIBE <http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389>
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http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389
http://www.w3.org/2000/01/rdf-schema#comment
"The ins776G mutation most likely causes a recessive triangular cataract with variable expressivity of a weak phenotype in heterozygotes."
xsd:string
http://purl.uniprot.org/uniprot/#_596B537CB6C0D69967D94EEB528064CA467C7F2DDE1EA51369BE2C5517A0610E26AA2638F87337B3C6DBE107718CB464
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389
http://purl.uniprot.org/uniprot/A0A097IW90
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389
http://purl.uniprot.org/uniprot/#_A0A097IW90-mappedCitation-18483562
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E61CA653F7F5A9F020D0CC694122EBFEFDC46E1A2CDDF840DECFF8B5E2B6465F5D857405FCAF854CA4D0C8BB1115E389