Barely Significant
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Vitamin D receptor gene polymorphism and polycystic ovary syndrome susceptibility.

BMC Med Genomics · 2023 · PMC10197246 · PMID 37202765

1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantP < 0.0001actually significant
The same results were obtained for the PCOS phenotype groups as a highly significant risk association was observed between phenotypes A, C, and D compared with that in the control group ( P < 0.0001).

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