Barely Significant
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Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.

Psychiatry Clin Neurosci · 2019 · PMC7380025 · PMID 30367527

1
hedged sentence
0.0013
closest p · 0.0× alpha
0.0013
boldest claim

The sentences

nominally significantP = 0.0013actually significant
In the ‘protein domains’ category tested using the Interpro database as the source, the term ‘epidermal growth factor like domain’ showed a nominally significant enrichment with P = 0.0013, Benjamini–Hochberg false discovery rate corrected P = 0.073.

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