Barely Significant
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Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome.

Orphanet J Rare Dis · 2023 · PMC10594698 · PMID 37872602

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closest p
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possibly significantno p-value reported
A smaller value of weight indicates a large T-value, which can be interpreted as a possibly significant level of gene expression, and vice versa.

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