Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP87576.RAuR9PHjwPnyZ3sjCBKJ0qXDSX2xBDzitXmC8FpyEsJO8130_assertion description "[To investigate the possible association between the glutamate-cysteine ligase catalytic subunit gene (GCLC) C-129T and modifier subunit gene (GCLM) G-23T polymorphisms with coronary heart disease (CHD) in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87576.RAuR9PHjwPnyZ3sjCBKJ0qXDSX2xBDzitXmC8FpyEsJO8130_provenance.
- NP87577.RAuAWHWvzt--pZmuYya3qvf4RNtI1gi-YvUB5swgFedpw130_assertion description "[Association study between hypertension and A/G polymorphism at codon 637 of the transporter associated with antigen processing 1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87577.RAuAWHWvzt--pZmuYya3qvf4RNtI1gi-YvUB5swgFedpw130_provenance.
- NP87579.RAvCmjKRcKAlJDYgPZN6VAJCkRE7jjG4PpNFDy_4YmuIU130_assertion description "[Significance of transporter associated with antigen processing 2 (TAP2) gene polymorphisms in susceptibility to dengue viral infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87579.RAvCmjKRcKAlJDYgPZN6VAJCkRE7jjG4PpNFDy_4YmuIU130_provenance.
- NP87583.RAoE6MxGQR4WMpVTNTXwGOU7Bu2rIZ5ETHoms-lf-HgH4130_assertion description "[In this study, we tested the hypothesis that mutations in the GABRA1, GABRB3, and GABRG2 genes encoding the alpha1, beta3, and gamma subunits of the GABA(A) receptor are involved in familial primary dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87583.RAoE6MxGQR4WMpVTNTXwGOU7Bu2rIZ5ETHoms-lf-HgH4130_provenance.
- NP87584.RAhI7MtMwi3N_CmCBvaqW0fVZJ26bjrRPo5hx7wSzVbD0130_assertion description "[Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87584.RAhI7MtMwi3N_CmCBvaqW0fVZJ26bjrRPo5hx7wSzVbD0130_provenance.
- NP87585.RAuYWhDkQC1ctdnkuYGddPwVFYzRN8elklzfqe4_2eDjE130_assertion description "[In this study, we tested the hypothesis that mutations in the GABRA1, GABRB3, and GABRG2 genes encoding the alpha1, beta3, and gamma subunits of the GABA(A) receptor are involved in familial primary dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87585.RAuYWhDkQC1ctdnkuYGddPwVFYzRN8elklzfqe4_2eDjE130_provenance.
- NP87590.RAi9Y23h7n-zpM3TFYC3N0peIO0FgGtvD7ydo2w_XMgdQ130_assertion description "[Polymorphisms for vinyl chloride metabolism in French vinyl chloride workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87590.RAi9Y23h7n-zpM3TFYC3N0peIO0FgGtvD7ydo2w_XMgdQ130_provenance.
- NP87592.RAkXUuxdYsQ2VA2sGbe7nJ0cYOVMeW_gflpQn0P-kYR50130_assertion description "[Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87592.RAkXUuxdYsQ2VA2sGbe7nJ0cYOVMeW_gflpQn0P-kYR50130_provenance.
- NP87595.RArKEW7Il819ptXQeOO_U_lejWnYIe9PnN3du825emPCQ130_assertion description "[Effect of ABCB1 (MDR1) 3435C >T and 2677G >A,T polymorphisms and P-glycoprotein inhibitors on salivary digoxin secretion in congestive heart failure patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87595.RArKEW7Il819ptXQeOO_U_lejWnYIe9PnN3du825emPCQ130_provenance.
- NP87596.RAth6pd9SEOgFsfQWZP4slc0cHgM2rCJ3_O1LA47Tr3fc130_assertion description "[Evaluation of urinary CA19-9 levels in bladder cancer patients classified according to the combinations of Lewis and Secretor blood group genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87596.RAth6pd9SEOgFsfQWZP4slc0cHgM2rCJ3_O1LA47Tr3fc130_provenance.
- NP87597.RAputZZrVHtwqFEqQm2B6wZl70LnPsTSOLoS7h31WI3fI130_assertion description "[Polymorphism of MDR1 is one of the determinants of successful eradication of H.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87597.RAputZZrVHtwqFEqQm2B6wZl70LnPsTSOLoS7h31WI3fI130_provenance.
- NP87598.RAi5JyeiPRXLYfZpMhxjjOD5gq0i9m9MzzBCu_SGtlK0s130_assertion description "[Pharmacogenomic associations in ABCB1 and CYP3A5 with acute kidney injury and chronic kidney disease after myeloablative hematopoietic cell transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87598.RAi5JyeiPRXLYfZpMhxjjOD5gq0i9m9MzzBCu_SGtlK0s130_provenance.
- NP87602.RAm7Jme06Hbqwx25xPYLZNPgTe3CFg525khrfXwyhPfak130_assertion description "[The influence of C3435T polymorphism of ABCB1 gene on penetration of phenobarbital across the blood-brain barrier in patients with generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87602.RAm7Jme06Hbqwx25xPYLZNPgTe3CFg525khrfXwyhPfak130_provenance.
- NP87604.RAjWxHYFN4SoAITZ3_L8eeJBa5Q4dc0oB_49QbLxEUMug130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87604.RAjWxHYFN4SoAITZ3_L8eeJBa5Q4dc0oB_49QbLxEUMug130_provenance.
- NP87607.RAi733a-KhoyASzojKd0Fvu_fzcI7FcelNA640dwffh9k130_assertion description "[Our findings suggest that increased serum FSH levels in subjects with primary amenorrhea correlated to FSHR genotype at position -29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87607.RAi733a-KhoyASzojKd0Fvu_fzcI7FcelNA640dwffh9k130_provenance.
- NP87615.RAumH3u4oALYObk-8MSCUg3bStaDNGxT2tsJF0PDumJ1g130_assertion description "[PI3K/PTEN/AKT/mTOR pathway genetic variation predicts toxicity and distant progression in lung cancer patients receiving platinum-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87615.RAumH3u4oALYObk-8MSCUg3bStaDNGxT2tsJF0PDumJ1g130_provenance.
- NP87619.RAoTeM4v8M9TRNWHZOYNDpEKaecy0LgVHd1X_XYyvtXIs130_assertion description "[Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87619.RAoTeM4v8M9TRNWHZOYNDpEKaecy0LgVHd1X_XYyvtXIs130_provenance.
- NP87623.RAvz0RYFyTfyo2uNt58xAgbnWUiPqlxLncwkobFcZ5mng130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87623.RAvz0RYFyTfyo2uNt58xAgbnWUiPqlxLncwkobFcZ5mng130_provenance.
- NP87626.RAiGxLDywY2LWuDOhu9SHROXdrvPbV8eKhCnPyIsNPKKc130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87626.RAiGxLDywY2LWuDOhu9SHROXdrvPbV8eKhCnPyIsNPKKc130_provenance.
- NP87629.RAnq2X9IMEZTB9sRRQVp-iZ9PdlqoV6swd5okCll0rm64130_assertion description "[Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87629.RAnq2X9IMEZTB9sRRQVp-iZ9PdlqoV6swd5okCll0rm64130_provenance.
- NP87633.RAs5sZL_YB89rmdgh3LNN3wJVXfg6F0OTQ8kokhy48Jik130_assertion description "[Our data indicate that the minor G-allele of FOXO3A rs2802292 is associated with enhanced peripheral and hepatic insulin sensitivity in our small twin cohort, which may be mediated through increased FOXO3A mRNA expression, although no major metabolic impact of rs2802292 was found in the large Inter99 cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87633.RAs5sZL_YB89rmdgh3LNN3wJVXfg6F0OTQ8kokhy48Jik130_provenance.
- NP87636.RAiWQY0BgJv74uhk-D82uthsc5eJi-49fTMuJrXX682O8130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87636.RAiWQY0BgJv74uhk-D82uthsc5eJi-49fTMuJrXX682O8130_provenance.
- NP87638.RAhzKn3MFfERDPIkxmUjDzMEA5vUoduxncs_V3wYyTHAA130_assertion description "[Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87638.RAhzKn3MFfERDPIkxmUjDzMEA5vUoduxncs_V3wYyTHAA130_provenance.
- NP87640.RAiGfQWvvkcNb90ZzJr36aGTWP1t28-SOTfczfQlaImrI130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87640.RAiGfQWvvkcNb90ZzJr36aGTWP1t28-SOTfczfQlaImrI130_provenance.
- NP87652.RAhAGXsV_X91zUkYjCgipO9Rf-kpDonPAljETXopAuBSM130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87652.RAhAGXsV_X91zUkYjCgipO9Rf-kpDonPAljETXopAuBSM130_provenance.
- NP87653.RAnXUWrub3IH3Crct6vTULaWDF9t0Zh6XXa3SwnMC2-Io130_assertion description "[Allelic polymorphism of FMR1 gene CGG-repeat region in patients with impairment of natural and stimulated ovulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87653.RAnXUWrub3IH3Crct6vTULaWDF9t0Zh6XXa3SwnMC2-Io130_provenance.
- NP87660.RAvNegloWFI7tH1xC-Z6Ajg_iX2LzhSznD5FuD-okUQDY130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87660.RAvNegloWFI7tH1xC-Z6Ajg_iX2LzhSznD5FuD-okUQDY130_provenance.
- NP87663.RArsa9tlMuA7wdbtE_Tic-0OpTWmVbNGVkWaE4Usu56DE130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87663.RArsa9tlMuA7wdbtE_Tic-0OpTWmVbNGVkWaE4Usu56DE130_provenance.
- NP87665.RAtvYjakFwzCaq_r-IIcXa_2nCSHR4XlABDefh5OcBIXI130_assertion description "[The current analyses are a useful addition to the present literature and will make a valuable contribution to future meta-analyses. The candidate gene findings are consistent with a prior meta-analysis in suggesting that the effects of ADHD risk variants must, individually, be very small and/or include multiple rare alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87665.RAtvYjakFwzCaq_r-IIcXa_2nCSHR4XlABDefh5OcBIXI130_provenance.
- NP87669.RAvHAMG4gDpv8vVJmqDHrSadYM_PcAugR-gotiqxUFXJM130_assertion description "[Filaggrin mutations confer susceptibility to atopic dermatitis but not to asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87669.RAvHAMG4gDpv8vVJmqDHrSadYM_PcAugR-gotiqxUFXJM130_provenance.
- NP87685.RAqMb1Sc4YCFktnHBBuhRCjDfPo1Ac61L8c29vdbvnUnc130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87685.RAqMb1Sc4YCFktnHBBuhRCjDfPo1Ac61L8c29vdbvnUnc130_provenance.
- NP87687.RAt72UTl7jz9-UE3zY4SlO0K2ycub5xXKpeJ8KHI8B4bY130_assertion description "[This candidate gene analysis identified the potential role of genes operating through intermediate disease pathways to influence sleep apnea phenotypes, providing a framework for focusing future replication studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87687.RAt72UTl7jz9-UE3zY4SlO0K2ycub5xXKpeJ8KHI8B4bY130_provenance.
- NP87693.RAlseAFubh-g80VP-yVIuadBqfefYxyUggg7INRoe7yik130_assertion description "[This candidate gene analysis identified the potential role of genes operating through intermediate disease pathways to influence sleep apnea phenotypes, providing a framework for focusing future replication studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87693.RAlseAFubh-g80VP-yVIuadBqfefYxyUggg7INRoe7yik130_provenance.
- NP87697.RAqX297FdJwy4S15L7YFUfrESo3MWo_XUyITWiKnp588M130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87697.RAqX297FdJwy4S15L7YFUfrESo3MWo_XUyITWiKnp588M130_provenance.
- NP87704.RAiGoc97m3ypW6yz8GatBctqEsJAo2rDjZtpAcEMT_6tU130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87704.RAiGoc97m3ypW6yz8GatBctqEsJAo2rDjZtpAcEMT_6tU130_provenance.
- NP87716.RAvz8D0FmMjOwqbvGrlx77pueXsbLPc-tLNiv_MiZjmxI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87716.RAvz8D0FmMjOwqbvGrlx77pueXsbLPc-tLNiv_MiZjmxI130_provenance.
- NP87725.RAgZuaAydCYbWnOMO1OYL6Pa0NGcKahxiFeHoIPAYZgjQ130_assertion description "[Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87725.RAgZuaAydCYbWnOMO1OYL6Pa0NGcKahxiFeHoIPAYZgjQ130_provenance.
- NP87740.RAgI0NEesXHgV6R41wwCZ74i0yN15Hkhvg-A37_sKGYOg130_assertion description "[Genotypes of NK cell KIR receptors, their ligands, and Fc receptors in the response of neuroblastoma patients to Hu14.18-IL2 immunotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87740.RAgI0NEesXHgV6R41wwCZ74i0yN15Hkhvg-A37_sKGYOg130_provenance.
- NP87743.RAr6oWxILHs3pwvaMiYRgpDPlaOtut-yyk9_bALkyHNSw130_assertion description "[Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87743.RAr6oWxILHs3pwvaMiYRgpDPlaOtut-yyk9_bALkyHNSw130_provenance.
- NP87746.RAj2wUbx_58eD8gU-_066oHGeBnCycROTHVLev-g9UlqA130_assertion description "[We detected weak but reproducible association with markers in several genes, in proximity to susceptibility loci found in previous GWAS studies of bipolar disorder. Further work is required to study their localization, expression, and regulation and international meta-analytic efforts will help to further elucidate their role.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87746.RAj2wUbx_58eD8gU-_066oHGeBnCycROTHVLev-g9UlqA130_provenance.
- NP87758.RAkf6jeO-4WDkkPKEjJA2NbnlJZ-uF2uSI_lcBi4uxkGg130_assertion description "[Despite the small sample size, this novel analysis method identified an sMRI component including brain areas previously reported to be abnormal in schizophrenia and an associated genetic component containing several putative schizophrenia risk genes. Thus, we identified multiple genes potentially underlying specific structural brain abnormalities in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87758.RAkf6jeO-4WDkkPKEjJA2NbnlJZ-uF2uSI_lcBi4uxkGg130_provenance.
- NP87759.RAuwmQGWOIm35W9pkBaBsV1bSYUTU0N9eWzxef_hKJFlk130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The developed amplification strategy allows for the pooling of multiple patients with non-overlapping phenotypes, enabling many patients to be analyzed simultaneously in a fast and cost-effective manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87759.RAuwmQGWOIm35W9pkBaBsV1bSYUTU0N9eWzxef_hKJFlk130_provenance.
- NP87763.RAlrc9g8kPtn38hAXkREKq9xZMN9LXxdKgn3HiGjDK36c130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87763.RAlrc9g8kPtn38hAXkREKq9xZMN9LXxdKgn3HiGjDK36c130_provenance.
- NP87765.RApoKKQFTKz4b7d8Z0deVNzKrjzZQiQ5VGkrZeaumdgiA130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87765.RApoKKQFTKz4b7d8Z0deVNzKrjzZQiQ5VGkrZeaumdgiA130_provenance.
- NP87766.RAn7PlCp9Jsk7VPFxpq-5NmlywdINzTK7EEA_R1M9O8oU130_assertion description "[We genotyped rs174553, rs99780, rs174575, and rs174583 in FADS1/FADS2, analyzed blood lipid fatty acids and assessed PPD risk as an Edinburgh Postnatal Depression Scale (EPDS) score > or =10 for 69 pregnant women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87766.RAn7PlCp9Jsk7VPFxpq-5NmlywdINzTK7EEA_R1M9O8oU130_provenance.
- NP87770.RAql-LK6v3k923zV2taIvUd3d2pyOV2HSfl2n91OMufxo130_assertion description "[Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87770.RAql-LK6v3k923zV2taIvUd3d2pyOV2HSfl2n91OMufxo130_provenance.
- NP87771.RAo2tStWdxL8W-8DJ-QSgky0dP9e6_QvouiXVorUn9cao130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87771.RAo2tStWdxL8W-8DJ-QSgky0dP9e6_QvouiXVorUn9cao130_provenance.
- NP87774.RAiFJUN66ujCqSqKFfsd7wtfg80B44hmdIUbFB2ToF1No130_assertion description "[Genetic variation of the FADS1 FADS2 gene cluster and n-6 PUFA composition in erythrocyte membranes in the European Prospective Investigation into Cancer and Nutrition-Potsdam study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87774.RAiFJUN66ujCqSqKFfsd7wtfg80B44hmdIUbFB2ToF1No130_provenance.
- NP87781.RAr98gj_be879XYORuUU-up9MA9_yrxI_473SVtkvd3xY130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87781.RAr98gj_be879XYORuUU-up9MA9_yrxI_473SVtkvd3xY130_provenance.
- NP87782.RAqal07VAhkP5T_PhOtYxbbduIfV1Bh2bTV2h5Bc0L90k130_assertion description "[These results suggest that these SNPs may not be useful in predicting colorectal cancer risk in populations with high fat intake.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87782.RAqal07VAhkP5T_PhOtYxbbduIfV1Bh2bTV2h5Bc0L90k130_provenance.
- NP87783.RAs5E72lJb9YEqcqjj_yzaxuVZMQaEE0R7c8xrGQUFMOg130_assertion description "[A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87783.RAs5E72lJb9YEqcqjj_yzaxuVZMQaEE0R7c8xrGQUFMOg130_provenance.
- NP87784.RAs4XSsS_PndlqyKKY3KMGei4NEUyyBsO6r3m14TY2NUM130_assertion description "[Overall, there is no conclusive evidence that genetic variants in genes involved in the estrogen metabolic pathway are associated with mammographic density in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87784.RAs4XSsS_PndlqyKKY3KMGei4NEUyyBsO6r3m14TY2NUM130_provenance.
- NP87788.RAhYrEUzi4CKVCjr0X0af4i2tsEidR0nN-UE7p-4C1EwM130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87788.RAhYrEUzi4CKVCjr0X0af4i2tsEidR0nN-UE7p-4C1EwM130_provenance.
- NP87793.RApD2TkBTjeZbgBes6MIn6nB58hf95u05esFisVeCRWng130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87793.RApD2TkBTjeZbgBes6MIn6nB58hf95u05esFisVeCRWng130_provenance.
- NP87796.RAhac34AoZ5KnuvY0IDDZS2qZAq7oGpJI0u-mt72T_efI130_assertion description "[The combination of prothrombotic polymorphisms may help to predict MI in patients with advanced CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87796.RAhac34AoZ5KnuvY0IDDZS2qZAq7oGpJI0u-mt72T_efI130_provenance.
- NP87797.RAiHTmZZSuVBHW9zfLFqo6jopMrhk6-8k9B-EpP4zmsv0130_assertion description "[Genetic susceptibility, smoking, obesity and risk of venous thromboembolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87797.RAiHTmZZSuVBHW9zfLFqo6jopMrhk6-8k9B-EpP4zmsv0130_provenance.
- NP87804.RAtWHpF1BD9Uz0_6Mfei1CC16OWve9mCmn1uP-MHVBNYE130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87804.RAtWHpF1BD9Uz0_6Mfei1CC16OWve9mCmn1uP-MHVBNYE130_provenance.
- NP87805.RAiJpwDhtmfL8ku54Q-2tDBvu90B9uzxyzLfJ0n88I_ss130_assertion description "[These studies identify single locus associations with preterm birth for both maternal and fetal genotypes in two populations of European ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87805.RAiJpwDhtmfL8ku54Q-2tDBvu90B9uzxyzLfJ0n88I_ss130_provenance.
- NP87806.RAlznzGnPjRvqM7Ptxf-iLhNYQi_Sr147NDkC9WgcShd8130_assertion description "[Cyclooxygenase-1 -842G and 50T alleles significantly contribute to the risk of bleeding complications in patients undergoing elective CAG. Genetic testing is able to influence the safety of diagnostic cardiac catheterization in large numbers of low risk patients with borderline indications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87806.RAlznzGnPjRvqM7Ptxf-iLhNYQi_Sr147NDkC9WgcShd8130_provenance.
- NP87810.RAuf3dyXbeD0Q6plmafhxHpHnmuTOsI6ZTih8QyNtPMjc130_assertion description "[Relative to non-carriers of normal BMI, the joint effect of factor V Leiden and obesity led to a 7.9-fold increased risk (OR(adj) 7.86, 95% CI 4.70-13.15); for prothrombin 20210A this was a 6.6-fold increased risk (OR(adj) 6.58, 95% CI 2.31-18.69).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87810.RAuf3dyXbeD0Q6plmafhxHpHnmuTOsI6ZTih8QyNtPMjc130_provenance.
- NP87826.RAhtFckE06o6TO4KX-HFm0EpWdLeFc5JiNORboq7FaSxE130_assertion description "[Gene variants associated with venous thrombosis: confirmation in the MEGA study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87826.RAhtFckE06o6TO4KX-HFm0EpWdLeFc5JiNORboq7FaSxE130_provenance.
- NP87829.RApwwsG8L5pxrGF_1gxGyMvQYj8m39ei1VqIWdtjoluBc130_assertion description "[The chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that six polymorphisms of F10, PITRM1, PCSK2, JPH3, MYO7B, and AKAP12 were related (P<0.05) to the prevalence of CKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87829.RApwwsG8L5pxrGF_1gxGyMvQYj8m39ei1VqIWdtjoluBc130_provenance.
- NP87830.RAukbG5r7VFgEfHckuOPaFmedGLYSvtm6OTrdz90QZHeQ130_assertion description "[, PZ plasma level is not a key player in the pathophysiology of premature coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87830.RAukbG5r7VFgEfHckuOPaFmedGLYSvtm6OTrdz90QZHeQ130_provenance.
- NP87833.RAsZDUJmJ7VCoANArLiEBpazwpcZTJYRv6SI3PkSlTub4130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87833.RAsZDUJmJ7VCoANArLiEBpazwpcZTJYRv6SI3PkSlTub4130_provenance.
- NP87839.RAg98iDrgDpT_DO6nzijj6S7i-P409MUAi_r4-TS-ptCA130_assertion description "[From these preliminary data, these polymorphisms would be candidates predicting the clinicopathological features of colorectal cancer, but further more systematic gene analyses are warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87839.RAg98iDrgDpT_DO6nzijj6S7i-P409MUAi_r4-TS-ptCA130_provenance.
- NP87840.RAr11NJ4NtccFM-wboR90YQOFGAHQtx_XE7Vs1TaxS5IA130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87840.RAr11NJ4NtccFM-wboR90YQOFGAHQtx_XE7Vs1TaxS5IA130_provenance.
- NP87841.RAmMoxhUO-4hdMvQpqSgsN9Fg-BwkPqNIU0dRlOb6vX38130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87841.RAmMoxhUO-4hdMvQpqSgsN9Fg-BwkPqNIU0dRlOb6vX38130_provenance.
- NP87845.RAg9QTKyRqRMg67bPOv9FepT8aDf9_y1JNiKOVABNUlp8130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87845.RAg9QTKyRqRMg67bPOv9FepT8aDf9_y1JNiKOVABNUlp8130_provenance.
- NP87855.RAj_ujhPJl-BB4RNslk7VEmxk28klryoY0F8S9msmVxVE130_assertion description "[Our results suggest that ESR1 gene polymorphisms may be associated with dysmenorrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87855.RAj_ujhPJl-BB4RNslk7VEmxk28klryoY0F8S9msmVxVE130_provenance.
- NP87870.RAkAkbMQcSC9RVsuG_brKhJ4SGZOYOmGto0zAJAVuBdCk130_assertion description "[Variation within DNA repair pathway genes and risk of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87870.RAkAkbMQcSC9RVsuG_brKhJ4SGZOYOmGto0zAJAVuBdCk130_provenance.
- NP87877.RAmtsWiTv5JfXEUi0GW2xVb4Hyuv9zKe81Gdoo3Ew48vU130_assertion description "[Assessments of the effects of smoking, alcohol, human papillomavirus and race/ethnicity on the association between DNA repair gene polymorphisms and head and neck cancer are needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87877.RAmtsWiTv5JfXEUi0GW2xVb4Hyuv9zKe81Gdoo3Ew48vU130_provenance.
- NP87887.RAq1etGBRlhpQfrq5xLspYhDJGRtoukP15kBrkpakpM8M130_assertion description "[The detection of somatic mutations in rectal cancer tumors led us to re-evaluate the utility of the tests performed in blood samples for these polymorphisms in rectal cancer. Furthermore, studies aimed at assessing the influence of pharmacogenetic markers in treatment response performed in blood samples should take into account the particular pattern of hypermutability present in each tumor type. We hypothesize that different patterns of hypermutability present in each tumor type would be related to the different results in association studies related to response to the treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87887.RAq1etGBRlhpQfrq5xLspYhDJGRtoukP15kBrkpakpM8M130_provenance.
- NP87889.RAsv3pnr-gP8T-z0A1EFFC71B1KM3zgnuzzmaj10eyoj8130_assertion description "[Associations between oxaliplatin-induced peripheral neuropathy and polymorphisms of the ERCC1 and GSTP1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87889.RAsv3pnr-gP8T-z0A1EFFC71B1KM3zgnuzzmaj10eyoj8130_provenance.
- NP87890.RAgRmdpyktcF11DC6XtVj4KxyenV-tCeTTkhEfDhf3jOc130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87890.RAgRmdpyktcF11DC6XtVj4KxyenV-tCeTTkhEfDhf3jOc130_provenance.
- NP87900.RAokXSSU8BJMa2Wb0gG_xnkTlQ74TGXgaeEfwD2tqai2M130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87900.RAokXSSU8BJMa2Wb0gG_xnkTlQ74TGXgaeEfwD2tqai2M130_provenance.
- NP87903.RAmhNVSfXVxzyofvhtWwp0wF4oP6Im91LMxpSbBhUO7dM130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87903.RAmhNVSfXVxzyofvhtWwp0wF4oP6Im91LMxpSbBhUO7dM130_provenance.
- NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_assertion description "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87913.RAjth6msSGDrqQYxLz0gev940d_WnovBXE-oEZh7t6AXI130_provenance.
- NP87915.RAsVvobJTT3_ULPo52SMZqzkZqaL9L9P4pAgP2-UQlcsM130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87915.RAsVvobJTT3_ULPo52SMZqzkZqaL9L9P4pAgP2-UQlcsM130_provenance.
- NP87918.RAvtbUgNi2XcUp4vxbpfGW_Fdzsq4I50Zj2LAYF4gBu3M130_assertion description "[Angiotensin II type 1 receptor 1166C polymorphism is associated with abdominal aortic aneurysm in three independent cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87918.RAvtbUgNi2XcUp4vxbpfGW_Fdzsq4I50Zj2LAYF4gBu3M130_provenance.
- NP87920.RAvzK-oSlFbnuVku0kn4lisAPf7YGSJK3ZI2zOzo_r20E130_assertion description "[Analysis of morpho-functional parameters of the heart and polymorphisms of Renin-Angiotensin-aldosterone system genes in patients with different variants of the course of hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87920.RAvzK-oSlFbnuVku0kn4lisAPf7YGSJK3ZI2zOzo_r20E130_provenance.
- NP87924.RAv4TP9d0Pk98gD2oiHngG3N4Zk7xjEPBTnQfOfYumAqE130_assertion description "[Our study could not confirm the findings by Biller and colleagues other than the influence of the ACE I/D polymorphism on serum ACE levels in both sarcoidosis patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87924.RAv4TP9d0Pk98gD2oiHngG3N4Zk7xjEPBTnQfOfYumAqE130_provenance.
- NP87925.RAgIM2VrDaN2Gd9K3BJUaKQuYQX-zQgSl1YBJ9cPqGgpg130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87925.RAgIM2VrDaN2Gd9K3BJUaKQuYQX-zQgSl1YBJ9cPqGgpg130_provenance.
- NP87932.RAmZyAZdmHe9hCNOto7TtPvzhMbJy2z3x6nUg8VJUXkNs130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87932.RAmZyAZdmHe9hCNOto7TtPvzhMbJy2z3x6nUg8VJUXkNs130_provenance.
- NP87934.RArYdFJuZMcE2siwToCjbO2UWV344qd9ySImqaofQvWFA130_assertion description "[Common polymorphisms in genes responsible for vascular function, inflammation, and oxidative stress appear to modify associations between proximity to major roadways and LVM. Further understanding of how genes modify effects of air pollution on CVD may help guide research efforts into specific mechanistic pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87934.RArYdFJuZMcE2siwToCjbO2UWV344qd9ySImqaofQvWFA130_provenance.
- NP87935.RAqMxZFMQez9eMuJEXkdOJ_WGT9Jiz_73IP_hw71KfKHI130_assertion description "[These data suggest that genetic polymorphisms in the renin-angiotensin system are associated with renal phenotypes in the general population, but that many associations differ across racial/ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87935.RAqMxZFMQez9eMuJEXkdOJ_WGT9Jiz_73IP_hw71KfKHI130_provenance.
- NP87944.RAipBWFm3ywaMxXj2CvlYiW9bj2ggXeNc0Sj13U1a55Ok130_assertion description "[It can be said that the angiotensinogen MT and AT1R CC1166 genotype carriers may have more risk than other genotypes in the development of hypertension in acromegaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87944.RAipBWFm3ywaMxXj2CvlYiW9bj2ggXeNc0Sj13U1a55Ok130_provenance.
- NP87947.RAoBVBCDTEtIKX4gkccOXoc3Rqiub9eGeP3YpCsCNrDn0130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87947.RAoBVBCDTEtIKX4gkccOXoc3Rqiub9eGeP3YpCsCNrDn0130_provenance.
- NP87952.RAhmGa8vY8XwukSfVcwEWjKFnoqkAACOIKB9OaryyBwXI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87952.RAhmGa8vY8XwukSfVcwEWjKFnoqkAACOIKB9OaryyBwXI130_provenance.
- NP87956.RAr-kk14_GyphrWGiHh6qbFhdTBTBtsGd06Y3631yAsIU130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87956.RAr-kk14_GyphrWGiHh6qbFhdTBTBtsGd06Y3631yAsIU130_provenance.
- NP87958.RAokqxHp1DhfmOVQxaSBPxbw-CCb_gvfBBTQe7fGowMpk130_assertion description "[This finding suggests that the AGO1 rs636832A>G might be a useful marker for determining the susceptibility to lung cancer and that the AGO1 gene might be involved in the development of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87958.RAokqxHp1DhfmOVQxaSBPxbw-CCb_gvfBBTQe7fGowMpk130_provenance.
- NP87962.RAt3Cr7e6hNbF-k6bjPXEO4t2rCcJ6oOGeAoJZhGb57f0130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87962.RAt3Cr7e6hNbF-k6bjPXEO4t2rCcJ6oOGeAoJZhGb57f0130_provenance.
- NP87963.RAji1dYpRlSXZk5uff8ayBQPqE1PjnzyDQHko1X-ydLEU130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87963.RAji1dYpRlSXZk5uff8ayBQPqE1PjnzyDQHko1X-ydLEU130_provenance.
- NP87966.RAknuBHT-71ZgY72SxXg__ynNdgjeH-C_1tWDrngBr7iM130_assertion description "[EGR3 as a potential susceptibility gene for schizophrenia in Korea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87966.RAknuBHT-71ZgY72SxXg__ynNdgjeH-C_1tWDrngBr7iM130_provenance.
- NP87970.RAmvcEkoTe2xprl_c3lDLOUZ3d4XaeapfB-mYs_L15qlY130_assertion description "[EGR3 as a potential susceptibility gene for schizophrenia in Korea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87970.RAmvcEkoTe2xprl_c3lDLOUZ3d4XaeapfB-mYs_L15qlY130_provenance.
- NP87976.RAtmSnjyc6jzSTOTgC4fRPfUpc4DLL0aq_sTMTKBOBoWI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87976.RAtmSnjyc6jzSTOTgC4fRPfUpc4DLL0aq_sTMTKBOBoWI130_provenance.
- NP87978.RAjKvyM3BXfUJQFfRKPnhNd4TxeCdB5zyvy7t7nx6nWxU130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87978.RAjKvyM3BXfUJQFfRKPnhNd4TxeCdB5zyvy7t7nx6nWxU130_provenance.
- NP87979.RAkEKQX7elAiPJHdeJfbexw4ztRk_OEXdAwwApCm0HSKc130_assertion description "[Deletion of NFKBIA has an effect that is similar to the effect of EGFR amplification in the pathogenesis of glioblastoma and is associated with comparatively short survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87979.RAkEKQX7elAiPJHdeJfbexw4ztRk_OEXdAwwApCm0HSKc130_provenance.
- NP87980.RAnmDJFF-w2NUPvE0J2QlUJCzr2R4SBeCj2nGmJM2KVhM130_assertion description "[Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87980.RAnmDJFF-w2NUPvE0J2QlUJCzr2R4SBeCj2nGmJM2KVhM130_provenance.
- NP87982.RAsFdgCF0Nw9E12tUGYmSt-n3jl2V0WcEy_HplSIy7RJQ130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87982.RAsFdgCF0Nw9E12tUGYmSt-n3jl2V0WcEy_HplSIy7RJQ130_provenance.
- NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_assertion description "[The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87985.RAhzKPHwnLWvr0elHyN7Ef7whRDpT39f579qg1gkCTdOA130_provenance.