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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
Lung cancer
398articles
398mentions
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 60Germline variants and impact on lung cancer outcomes following chemotherapy: A systematic review.
PMID 42342141 | DOI 10.1016/j.critrevonc.2026.105453 · Critical reviews in oncology/hematology · 2026 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | lung cancer | “Germline variants and impact on lung cancer outcomes following chemotherapy: A systematic review.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | C118T | “Genetic variants associated with overall survival and/or progression-free survival included XPD Lys751Gln, XPD Asp312Asn, ERCC1 C118T, and XRCC1 Arg399Gln.” | 0.82 | literature_variant_regex_v2 |
| gene | ERCC1 | “Genetic variants associated with overall survival and/or progression-free survival included XPD Lys751Gln, XPD Asp312Asn, ERCC1 C118T, and XRCC1 Arg399Gln.” | 0.98 | hgnc_dict_v1 |
| gene | XRCC1 | “Genetic variants associated with overall survival and/or progression-free survival included XPD Lys751Gln, XPD Asp312Asn, ERCC1 C118T, and XRCC1 Arg399Gln.” | 0.98 | hgnc_dict_v1 |