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DESCRIBE <http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62>
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http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62
http://www.w3.org/2000/01/rdf-schema#comment
"Genome sequencing of the deletion breakpoints showed that the DLX5 and DLX6 genes are disomic but the putative DYNC1I1 exon 15 and 17 enhancers are deleted."
xsd:string
http://purl.uniprot.org/uniprot/#_A0E8B083668A4F60563ADA17D3309D92537C7C7A6B7963247E43E3457158F31EAE0CE3626C70E5F5F48B2CF52E17D8AD
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62
http://purl.uniprot.org/uniprot/Q8N542
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62
http://purl.uniprot.org/uniprot/#_Q8N542-mappedCitation-24459211
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4DC131746EDF76D4233D296072F0D1B0AC7AB629AF84242855A4C5DBFE398676A5B1337C15BC344AC055A6D453FF5E62