Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies.

Cancer Med · 2019 · PMC6434199 · PMID 30793520

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

Thirty‐eight variants were considered to be nominally significant associated with risk of EC or ESCC, whereas the rest showed non‐association.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.