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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
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
2 records shown · first 60Thrombophilia in young patients with acute myocardial infarction.
PMID 18176672 · Saudi medical journal · 2008 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | hypertension | “RESULTS: There were statistically significant differences in terms of obesity, smoking, triglyceride, total cholesterol, high-density lipoprotein, high-density lipoprotein, and very-low-density lipoprotein cholesterol, family history, hypertension, diabetes, and left ventricular hypertrophy between patients and controls.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | G20210A | “Traditional risk factors of CAD and protein C, S, antithrombin III deficiencies, factor V Leiden (FV Leiden), prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T mutations were investigated.” | 0.82 | literature_variant_regex_v2 |
| gene | MTHFR | “Traditional risk factors of CAD and protein C, S, antithrombin III deficiencies, factor V Leiden (FV Leiden), prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T mutations were investigated.” | 0.98 | hgnc_dict_v1 |
| phenotype | myocardial infarction | “Thrombophilia in young patients with acute myocardial infarction.” | 0.98 | phenotype_alias_lexicon_v2 |
Genetics of ischemic stroke.
PMID 21063358 · Neurosciences (Riyadh, Saudi Arabia) · 2008 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | hypertension | “Most cases of ischemic stroke are attributable to hypertension and other risk factors, but in over 20% of cases, the cause is unknown.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | G20210A | “Moreover, thrombophilic states such as prothrombin G20210A mutation and factor V Leiden are now known to cause arterial stroke as well as venous thrombosis.” | 0.82 | literature_variant_regex_v2 |
| gene | PDE4D | “Recent research has implicated some novel genes in the etiology of ischemic stroke, including genes for soluble epoxide hydrolase (sHE), 5-lipoxygenase activating protein (FLAP) and phosphodiesterase 4D (PDE4D).” | 0.98 | hgnc_dict_v1 |
| phenotype | stroke | “Genetics of ischemic stroke.” | 0.98 | phenotype_alias_lexicon_v2 |