Barely Significant
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Splicing Anomalies in Myeloproliferative Neoplasms: Paving the Way for New Therapeutic Venues.

Cancers (Basel) · 2020 · PMC7464941 · PMID 32784800

Europe PMCDOI
1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

close to being significantp = 0.06so close (0.05 < p ≤ 0.1)
[ 51 ], the association between SRSF2 mutations and transfusion requirement was close to being significant ( p = 0.06).

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