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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
Prostate cancer
218articles
218mentions
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 60Analyzing the mutational landscape of prostate cancer susceptibility genes through next-generation sequencing (NGS).
PMID 39398597 | PMCID PMC11470312 | DOI 10.62347/QRIF7244 · American journal of translational research · 2024 · 31 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | prostate cancer | “Analyzing the mutational landscape of prostate cancer susceptibility genes through next-generation sequencing (NGS).” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | c.5198A>G | “For the BRCA2 gene, one pathogenic mutation, c.6275_6276del (p.Val2092fs), was detected in 10 patients, and four benign mutations, c.5347A>T (p.Met1783Leu), c.5198A>G (p.Asp1733Gly), c.5158A>G (p.Thr1720Ala), and c.5117G>C (p.Gly1706Ala), were found in 17, 21, 34, and 12 patients, respectively.” | 0.95 | hgvs_regex_v1 |
| gene | BRCA1 | “RESULTS: Our study identified genetic mutations in BRCA1, BRCA2, TP53, and PMS2.” | 0.98 | hgnc_dict_v1 |
| gene | BRCA2 | “RESULTS: Our study identified genetic mutations in BRCA1, BRCA2, TP53, and PMS2.” | 0.98 | hgnc_dict_v1 |