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DESCRIBE <http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF>
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http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF
http://www.w3.org/2000/01/rdf-schema#comment
"This is the first report of an interstitial deletion encompassing OCRL and SMARCA1 gene in Lowe syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_F5C29B7D94E74A5670643CDBE2E73EB3E46A09CCA0246CCBE4DE7FA049007AEB1096415CB99EAF8CCC188B03C5D303D5
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF
http://purl.uniprot.org/uniprot/Q504W7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF
http://purl.uniprot.org/uniprot/#_Q504W7-mappedCitation-31376231
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B5A8BC6C9222E05B43FA5D27AED13081716E4494ED12A380BD8C563809067041A14E5060AA06445780B3D7D4FDC0D2CF