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- NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_assertion type Assertion NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_head.
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- NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_assertion wasDerivedFrom befree-20140225 NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_provenance.
- NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_assertion SIO_000772 16869734 NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_provenance.
- NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_assertion evidence source_evidence_literature NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_provenance.
- NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_assertion description "[These findings suggest that the AC and SCC subtypes may arise from a common cell of origin and they are driven to their distinct phenotypic end points by altered expression of a limited number of key genes such as p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549787.RAZKls-6lMGLd4IqgBoLxNjR8fyVgRBMYptOey6Mz7NIQ130_provenance.