Barely Significant
← all excerpts

Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X.

Nat Commun · 2014 · PMC4214414 · PMID 25307848

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
The P682S SNP demonstrated a highly significant association with the FCCTX phenotype resulting in an increased risk for CRC ( Table 3 ).

also in 132,142 other papers

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.