Barely Significant
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Specific allelic variants of SNPs in the <i>MDM2</i> and <i>MDMX</i> genes are associated with earlier tumor onset and progression in Caucasian breast cancer patients.

Oncotarget · 2019 · PMC6443004 · PMID 30956778

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highly significantno p-value reported
It must be emphasized that only four patients carried the C/C genotype (see above); nonetheless, the difference is highly significant.

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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.