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DESCRIBE <http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909>
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http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909
http://www.w3.org/2000/01/rdf-schema#comment
"A novel deletion in exon 3 of the RHO gene c.614-622del results in a classical form of retinitis pigmentosa in a multi-generation French family."
xsd:string
http://purl.uniprot.org/uniprot/#_6B758FFC54813EDDC99D08F3FABAB74D298D2F8251001008E94F29106D0557D8D7CF9C3C13C4586323262F65529CF890
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909
http://purl.uniprot.org/uniprot/V9H017
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909
http://purl.uniprot.org/uniprot/#_V9H017-mappedCitation-22419850
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A7957D605447ED148512AED7BC3859B2A1A759F7999E5A16A0F5A3605A80528DC9185C3DA687062B3A01744CCEA92909