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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
Myocardial infarction
274articles
274mentions
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 60Genetic Polymorphism in Angiotensinogen and Its Association with Cardiometabolic Diseases.
PMID 36557328 | PMCID PMC9785123 | DOI 10.3390/metabo12121291 · Metabolites · 2022 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | myocardial infarction | “Several cardiovascular diseases including myocardial infarction, coronary heart disease, heart failure, hypertrophy, etc. are associated with AGT polymorphism.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | T174M | “The most common variants of AGT polymorphism are M235T and T174M.” | 0.82 | literature_variant_regex_v2 |
| phenotype | obesity | “Other diseases such as depression, obesity, diabetic nephropathy, pre-eclampsia, and liver injury are also associated with some variants of AGT gene.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | pre-eclampsia | “Other diseases such as depression, obesity, diabetic nephropathy, pre-eclampsia, and liver injury are also associated with some variants of AGT gene.” | 0.98 | phenotype_alias_lexicon_v2 |