Barely Significant
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Nrf2 gene mutation and single nucleotide polymorphism rs6721961 of the Nrf2 promoter region in renal cell cancer.

BMC Cancer · 2019 · PMC6873559 · PMID 31752777

1
hedged sentence
0.1966
closest p · 3.9× alpha
0.1966
boldest claim

The sentences

did not reach statistical significancep = 0.1966not close (p > 0.1)
Keap1 gene mutations were also associated with shorter overall survival, but this association did not reach statistical significance ( p = 0.1966, Fig. 3 d), even after dividing the patients into a group with the C/C genotype of rs6721961 and a group with the C/A or A/A genotypes.

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