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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.

Publications

2 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
variantrs1421085“Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia.”0.90hgvs_regex_v1
geneFTO“Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia.”0.98hgnc_dict_v1
phenotypeobesity“Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia.”0.98phenotype_alias_lexicon_v2
phenotypeinfertility“Polycystic ovary syndrome (PCOS) is characterised by infertility, obesity, insulin resistance and clinical and/or biochemical signs of hyperandrogenism.”0.98phenotype_alias_lexicon_v2

Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population.

PMID 29466028 | DOI 10.1089/gtmb.2017.0218 · Genetic testing and molecular biomarkers · 2018 · 7 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs1421085“AIM: To identify novel mutations in the MC4R gene and to perform correlation analyses of the known variants rs9939609 and rs1421085 in the FTO gene and rs17782313 near the MC4R gene in an obese Saudi population.”0.90hgvs_regex_v1
geneFTO“Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population.”0.98hgnc_dict_v1
geneMC4R“Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population.”0.98hgnc_dict_v1
phenotypeobesity“Analysis of the Impact of Common Polymorphisms of the FTO and MC4R Genes with the Risk of Severe Obesity in Saudi Arabian Population.”0.98phenotype_alias_lexicon_v2