Barely Significant
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Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.

Int J Cancer · 2020 · PMC7004061 · PMID 31525256

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantp ‐value < 0.05actually significant
Pathway analysis for candidate genes arising from the family‐based association analysis with nominally significant association ( p ‐value < 0.05).

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