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DESCRIBE <http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31>
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http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31
http://www.w3.org/2000/01/rdf-schema#comment
"ETV6 and CDKN1B are mainly affected by small monoallelic deletions whereas mutations and hypermethylation play a minor role in CK-AML."
xsd:string
http://purl.uniprot.org/uniprot/#_C2177FC2244410A6D8E34F40E0A50278C58A07FC21CCC2D5623304DC29B63DD43099DF97F45039B63CA77B5F29F2B5E4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31
http://purl.uniprot.org/uniprot/P41212
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31
http://purl.uniprot.org/uniprot/#_P41212-mappedCitation-25213837
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B5306113EA89A0C588FBBECEBEC1AE681D0D43441E883D45105580CD6947DECD52D368BF44CE48B3A1BC5099F172FB31