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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.
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Phenotype
Hypertension
828articles
828mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60The mitochondrial DNA variant 16189T>C is associated with coronary artery disease and myocardial infarction in Saudi Arabs.
PMID 20143910 | DOI 10.1089/gtmb.2009.0095 · Genetic testing and molecular biomarkers · 2010 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | hypertension | “However, this association was influenced by age as well as the presence of myocardial infarction and hypertension.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | 16189T>C | “The mitochondrial DNA variant 16189T>C is associated with coronary artery disease and myocardial infarction in Saudi Arabs.” | 0.82 | literature_variant_regex_v2 |
| phenotype | coronary artery disease | “The mitochondrial DNA variant 16189T>C is associated with coronary artery disease and myocardial infarction in Saudi Arabs.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | myocardial infarction | “The mitochondrial DNA variant 16189T>C is associated with coronary artery disease and myocardial infarction in Saudi Arabs.” | 0.98 | phenotype_alias_lexicon_v2 |