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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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2 records shown · first 60

PMID 41383818 | PMCID PMC12689503 | DOI 10.3389/fnagi.2025.1676115 · Frontiers in aging neuroscience · 2025 · 4 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
variant	G2019S	“CONCLUSION: The absence of the LRRK2 and specifically the G2019S mutation in Emirati PD patients corroborates findings from Saudi Arabia and indicates a distinct genetic pattern compared to other Arab regions like Egypt and Maghreb (North African) countries, where the G2019S mutation prevalence ranges from 10 to 40%.”	0.82	literature_variant_regex_v2
gene	LRRK2	“Absence of the LRRK2 mutation in Emirati Parkinson's disease patients in contrast to other Arab populations.”	0.98	hgnc_dict_v1
phenotype	Parkinson disease	“Absence of the LRRK2 mutation in Emirati Parkinson's disease patients in contrast to other Arab populations.”	0.93	phenotype_alias_lexicon_v2
population	Saudi Arabia	“RESULTS: The LRRK2 mutation was not detected in any of the 50 Emirati PD patients (mean age 64.2 ± 14.1 years, of whom 56% are male) examined. CONCLUSION: The absence of the LRRK2 and specifically the G2019S mutation in Emirati PD patients corroborates findings from Saudi Arabia and indicates a distinct genetic pattern compared to other Arab regions like Egypt and Maghreb (North African) countries, where the G2019S mutation prevalence ranges from 10 to 40%.”	0.95	saudi_context_rules_v1

PMID 35147886 | DOI 10.1007/s11356-022-19082-5 · Environmental science and pollution research international · 2022 · 3 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
variant	G2019S	“G2019S is perhaps the maximum common mutation in PD subjects.”	0.82	literature_variant_regex_v2
gene	LRRK2	“Exploring the focal role of LRRK2 kinase in Parkinson's disease.”	0.98	hgnc_dict_v1
phenotype	Parkinson disease	“Exploring the focal role of LRRK2 kinase in Parkinson's disease.”	0.93	phenotype_alias_lexicon_v2