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- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion type Assertion NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_head.
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- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion wasDerivedFrom befree-20150227 NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_provenance.
- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion SIO_000772 21627674 NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_provenance.
- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion evidence source_evidence_literature NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_provenance.
- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_provenance.