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DESCRIBE <http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1>
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http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1
http://www.w3.org/2000/01/rdf-schema#comment
"Although reduced HDAC-activity facilitates oncogenic transformation in normal cells resulting tumor cells remain highly dependent on HDAC-activity indicating that a critical level of Hdac1 and Hdac2 is required for tumor maintenance."
xsd:string
http://purl.uniprot.org/uniprot/#_F0E19859E3175B0E2C368185A46F5D4D6A514BCDD3154D3CC337A7A1561551EB45AA45E89EC1C63B936B6D0F79B9E0DE
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1
http://purl.uniprot.org/uniprot/P70288
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1
http://purl.uniprot.org/uniprot/#_P70288-mappedCitation-23327920
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/9693625441D0ED2DC338F1F7F74BAB24A951D512BE7B3A4235AE3233E7AB11221B0D0A2AA7A0E67FC2A800DD47A61DC1