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DESCRIBE <http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99>
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http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99
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/#_1A52B1D4BDBE25F1035F58B5376F1C0BF00181FE718A890EE308D27B1D5394C9577CDDBA478B6C34B286FA17415F224C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99
http://purl.uniprot.org/uniprot/X5D7G1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99
http://purl.uniprot.org/uniprot/#_X5D7G1-mappedCitation-18483562
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1D22F0FCED6F08B06D37725A59D2755AE8BB7D2DD6772867E44DF5A2626EAFEA86D6E7ACFBE2E3B0A485AA53AD64FE99