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Combine gene, variant, phenotype, region and year filters

Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.

Publications

1 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
variantrs509504“Of the five reported variants, SNPs rs2483205 (OR = 1.429, 95% CI = 0.925-2.207, p = 0.061) and rs562556 (OR = 2.50, 95% CI = 1.274-4.906, p = 0.001) showed strong positive association with myocardial infarction (MI).Whereas SNPs rs540796, rs509504, and rs505151 (p > 0.05) showed no association with MI in the study population.”0.90hgvs_regex_v1
genePCSK9“Identification of genetic risk variants in PCSK9 gene and its association with myocardial infarction in Pakistani Pashtun population.”0.98hgnc_dict_v1
phenotypemyocardial infarction“Identification of genetic risk variants in PCSK9 gene and its association with myocardial infarction in Pakistani Pashtun population.”0.98phenotype_alias_lexicon_v2
variantrs2483205“Of the five reported variants, SNPs rs2483205 (OR = 1.429, 95% CI = 0.925-2.207, p = 0.061) and rs562556 (OR = 2.50, 95% CI = 1.274-4.906, p = 0.001) showed strong positive association with myocardial infarction (MI).Whereas SNPs rs540796, rs509504, and rs505151 (p > 0.05) showed no association with MI in the study population.”0.90hgvs_regex_v1