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http://purl.uniprot.org/SHA-384/F8780B8D6C1C2884275B6ABF3EA5431B7DAC1E941CA4002AD77B380C31DD355B246D1B6B97BE79DB0AD1C7D26FE5B2E7http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F8780B8D6C1C2884275B6ABF3EA5431B7DAC1E941CA4002AD77B380C31DD355B246D1B6B97BE79DB0AD1C7D26FE5B2E7http://www.w3.org/2000/01/rdf-schema#comment"Tumor cells bearing a p53 mutation showed increased damage levels and delayed repair. Knockdown of hnRNPK applied simultaneously with irradiation reduced colony-forming ability and survival of tumor cells. Taken together our data shows that hnRNPK is a relevant modifier of DNA damage repair and tumor cell survival. We therefore recommend further studies to evaluate the potential of hnRNPK as a drug target for improvement"xsd:string
http://purl.uniprot.org/uniprot/#_CF8BA14EBCB367349335AB7DD83888302E320D649FB9FEEC4B10816F1FAB76C403816EB6D5124B1895150F3E808CC200http://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/F8780B8D6C1C2884275B6ABF3EA5431B7DAC1E941CA4002AD77B380C31DD355B246D1B6B97BE79DB0AD1C7D26FE5B2E7
http://purl.uniprot.org/uniprot/B4DUQ1http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/F8780B8D6C1C2884275B6ABF3EA5431B7DAC1E941CA4002AD77B380C31DD355B246D1B6B97BE79DB0AD1C7D26FE5B2E7
http://purl.uniprot.org/uniprot/#_B4DUQ1-mappedCitation-28426877http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/F8780B8D6C1C2884275B6ABF3EA5431B7DAC1E941CA4002AD77B380C31DD355B246D1B6B97BE79DB0AD1C7D26FE5B2E7