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DESCRIBE <http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4>
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http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4
http://www.w3.org/2000/01/rdf-schema#comment
"the unique genotype identified in this study suggested that haploinsufficiencies of PAX6 or PRRG4 included in this region are candidate genes for severe developmental delay and autistic features characteristic of WAGR syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_FFEF170E9D054928E02A0225CE2E8C4E44970ADA45E0AEF04313F802A94206E8E4E8C07D5A07AE92F220BB71D03219CA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4
http://purl.uniprot.org/uniprot/Q9BZD6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4
http://purl.uniprot.org/uniprot/#_Q9BZD6-mappedCitation-24357251
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/11A5FFE1AE52AFCDD29EC773802E953DD6AF7BE79B408DF2072AD112E675CD0E03297B50A7C388ED0A443E58A39AD4F4