Barely Significant
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Human gene and disease associations for clinical-genomics and precision medicine research.

Clin Transl Med · 2020 · PMC7240856 · PMID 32508008

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highly significantno p-value reported
Gene‐disease data are highly significant at every level of biological research and healthcare but with inconsistencies and inabilities in terms of gene annotation, specificity of disease classification terminologies adds to the complexity and lack of an efficient integrative searchable system that makes it difficult to comprehend the underlying implications.

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