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http://purl.uniprot.org/SHA-384/E7DF3AF8909B1209644BF14AD3BA0AACE556A3C51D482F5C71A78D5C9BDA266BBF97AFE4E7C629FD9CF98E6A66924863http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E7DF3AF8909B1209644BF14AD3BA0AACE556A3C51D482F5C71A78D5C9BDA266BBF97AFE4E7C629FD9CF98E6A66924863http://www.w3.org/2000/01/rdf-schema#comment"Due to the multifunctionality of CENP-F the cellular phenotypes observed upon its depletion are difficult to interpret and there is a need to genetically separate its different functions by preventing binding to selected partners. Here we engineer a CENP-F point-mutant that is deficient in Miro1/2 binding and thus is unable to localize to mitochondria but retains other localizations."xsd:string
http://purl.uniprot.org/uniprot/#_AACAB2F393B199E7205B11FE92B6364AD5BBDA63D5443A02F39C7C2B870EE0FA07304DE4758CCBA5D2F43A4B14AB1DA5http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/E7DF3AF8909B1209644BF14AD3BA0AACE556A3C51D482F5C71A78D5C9BDA266BBF97AFE4E7C629FD9CF98E6A66924863
http://purl.uniprot.org/uniprot/Q9CUL0http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/E7DF3AF8909B1209644BF14AD3BA0AACE556A3C51D482F5C71A78D5C9BDA266BBF97AFE4E7C629FD9CF98E6A66924863
http://purl.uniprot.org/uniprot/#_Q9CUL0-mappedCitation-30856164http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/E7DF3AF8909B1209644BF14AD3BA0AACE556A3C51D482F5C71A78D5C9BDA266BBF97AFE4E7C629FD9CF98E6A66924863