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DESCRIBE <http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC>
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http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC
http://www.w3.org/2000/01/rdf-schema#comment
"Data show that the minor allele (N) of I393N in IQCB1 and the common allele (R) of R744Q in RPGRIP1L were associated with severe disease in XlRP with RPGR mutations."
xsd:string
http://purl.uniprot.org/uniprot/#_FEEFE0C10942B2807738B82157D64964655B72F3B82603378C2AB672EE18C85B846BCA917869454F129DE965D6DE2AB8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC
http://purl.uniprot.org/uniprot/Q68CZ1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC
http://purl.uniprot.org/uniprot/#_Q68CZ1-mappedCitation-21857984
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CAA921405A098A42B51EFC8E460C7CDA73D6B7AADBB9256DB441CD8FA9A3B0E2F8BEBF8E74B0A08D743FE48FA4125ECC