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- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_assertion type Assertion NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_head.
- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_assertion wasGeneratedBy ECO_0000203 NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_provenance.
- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_assertion wasDerivedFrom befree-2016 NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_provenance.
- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_assertion SIO_000772 9627113 NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_provenance.
- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_assertion evidence source_evidence_literature NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_provenance.
- NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_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." NP1397397.RAVQ6Kd9TfykM-ORJ38G79OfIdt5d6GH97Je7RnTen58w130_provenance.