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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
Turner syndrome
23articles
23mentions
10co-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 60Brain-derived neurotrophic factor G196A (rs6265) gene polymorphism increases Turner syndrome susceptibility.
PMID 36597258 | DOI 10.1080/02648725.2022.2164417 · Biotechnology & genetic engineering reviews · 2023 · 4 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | Turner syndrome | “Brain-derived neurotrophic factor G196A (rs6265) gene polymorphism increases Turner syndrome susceptibility.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | G196A | “Brain-derived neurotrophic factor G196A (rs6265) gene polymorphism increases Turner syndrome susceptibility.” | 0.82 | literature_variant_regex_v2 |
| gene | BDNF | “Brain-derived neurotrophic factor (BDNF) is a member of the nerve growth factor family.” | 0.98 | hgnc_dict_v1 |
| variant | rs6265 | “Brain-derived neurotrophic factor G196A (rs6265) gene polymorphism increases Turner syndrome susceptibility.” | 0.90 | hgvs_regex_v1 |