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http://purl.uniprot.org/SHA-384/50E83D06D047B9346192F2FC4F0893D834B2C5D939E2DB7CD072392D68382DD22DD1CEA9F5E8EB3B71F0B9D0A768D257http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/50E83D06D047B9346192F2FC4F0893D834B2C5D939E2DB7CD072392D68382DD22DD1CEA9F5E8EB3B71F0B9D0A768D257http://www.w3.org/2000/01/rdf-schema#comment"The subcellular distributions of IkappaB and NFkappaB are indicative of carcinogenesis. Inhibition of XPO1 results in intranuclear retention of IkappaB which inhibits NFkappaB and thereby provides a novel mechanism for drug therapy in sarcoma. This effect can be further enhanced in relatively selinexor-resistant sarcoma cell lines by pretreatment with the proteasome inhibitor carfilzomib."xsd:string
http://purl.uniprot.org/uniprot/#_512988C80CFF9B42067B85D0A698A0115E4D12A9A77CBFF897914107A8642CFAFFE9A58F668E7342608C9AD2891E381Chttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/50E83D06D047B9346192F2FC4F0893D834B2C5D939E2DB7CD072392D68382DD22DD1CEA9F5E8EB3B71F0B9D0A768D257
http://purl.uniprot.org/uniprot/A0A7I2V6B9http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/50E83D06D047B9346192F2FC4F0893D834B2C5D939E2DB7CD072392D68382DD22DD1CEA9F5E8EB3B71F0B9D0A768D257
http://purl.uniprot.org/uniprot/#_A0A7I2V6B9-mappedCitation-28314790http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/50E83D06D047B9346192F2FC4F0893D834B2C5D939E2DB7CD072392D68382DD22DD1CEA9F5E8EB3B71F0B9D0A768D257