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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
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.1129C>T | “In the TP53 gene, we found two pathogenic mutations, c.1014_1015insT (p.Glu339Ter) and c.916C>T (p.Arg306Ter), in 10 and 11 patients, respectively, and two benign mutations, c.311T>C (p.Ser104Pro) and c.1129C>T (p.Arg377Cys), in 8 and 9 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 |