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- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion type Assertion NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_head.
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- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion wasDerivedFrom befree-20150227 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion SIO_000772 9627113 NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion evidence source_evidence_literature NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.
- NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_assertion description "[Investigation of mutations in exon 8, especially codon 273 mutation and mutant H2 alpha helix was considered to be a clinically useful approach for determining the prognosis of patients with NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964246.RAT6uXZvCEK6DMnJFTQkry__03DSEOvSZVOwspivqLxYY130_provenance.