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

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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.

1 records shown · first 60

PMID 41922505 | PMCID PMC13184031 | DOI 10.1038/s41598-026-44969-5 · Scientific reports · 2026 · 6 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
phenotype	myocardial infarction	“Association of P2Y12 G52T genetic polymorphism with recurrent thromboembolic events in stroke and myocardial infarction patients on clopidogrel therapy: a prospective observational study.”	0.98	phenotype_alias_lexicon_v2
variant	G52T	“Association of P2Y12 G52T genetic polymorphism with recurrent thromboembolic events in stroke and myocardial infarction patients on clopidogrel therapy: a prospective observational study.”	0.82	literature_variant_regex_v2
phenotype	stroke	“Association of P2Y12 G52T genetic polymorphism with recurrent thromboembolic events in stroke and myocardial infarction patients on clopidogrel therapy: a prospective observational study.”	0.98	phenotype_alias_lexicon_v2
phenotype	hypertension	“Clopidogrel response is influenced by genetic factors as well as non-genetic factors such as obesity, hypertension, diabetes mellitus, age, gender, social habits, and drug-drug interactions.”	0.98	phenotype_alias_lexicon_v2