Barely Significant
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Structural heart defects associated with ET<sub>B</sub> mutation, a cause of Hirschsprung disease.

BMC Cardiovasc Disord · 2021 · PMC8487587 · PMID 34600481

1
hedged sentence
0.2500
closest p · 5.0× alpha
0.2500
boldest claim

The sentences

did not reach statistical significancep value = 0.25not close (p > 0.1)
Volumetric measurement of AA also showed 22.00% reduction in sl/sl rats with respect to the control; however, this finding did not reach statistical significance, p value = 0.25.

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