Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP89561.RAmbW4DQm9ichApwSYbpy42xv12NVw9Sy4MMiHG_QotcI130_assertion description "[A heterogeneous collection of THAP1 sequence variants is associated with varied anatomical distributions and onset ages of both familial and sporadic primary dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89561.RAmbW4DQm9ichApwSYbpy42xv12NVw9Sy4MMiHG_QotcI130_provenance.
- NP89564.RAsqKeSowqcIKTimqyn5TwJp-BGsBF141GOv43snXiaVc130_assertion description "[In addition, we report here five new loci for prostate cancer susceptibility, at 5p15 (lambda-corrected probability P(GC) = 3.9 x 10(-18)), GPRC6A/RFX6 (P(GC) = 1.6 x 10(-12)), 13q22 (P(GC) = 2.8 x 10(-9)), C2orf43 (P(GC) = 7.5 x 10(-8)) and FOXP4 (P(GC) = 7.6 x 10(-8)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89564.RAsqKeSowqcIKTimqyn5TwJp-BGsBF141GOv43snXiaVc130_provenance.
- NP89565.RAmKu3QS5OhSAOO6LAV8u1s0orAb2gi6EDutyvMcdWRvI130_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." NP89565.RAmKu3QS5OhSAOO6LAV8u1s0orAb2gi6EDutyvMcdWRvI130_provenance.
- NP89566.RAnTOxK6QvleWWFkntHXZfjui73N5tsIHcNnUNbzAHnC8130_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." NP89566.RAnTOxK6QvleWWFkntHXZfjui73N5tsIHcNnUNbzAHnC8130_provenance.
- NP89571.RArjX1peJU993UccReQlRs1HWL8JAkRn42HxmnjhRYTcQ130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89571.RArjX1peJU993UccReQlRs1HWL8JAkRn42HxmnjhRYTcQ130_provenance.
- NP89575.RAhKnc2DcKICGjtSMQfWHFh_jXOT7PN4PNP2b2XteLHYo130_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." NP89575.RAhKnc2DcKICGjtSMQfWHFh_jXOT7PN4PNP2b2XteLHYo130_provenance.
- NP89580.RAophiDz554QqpmvOZcSBy4v0ios6dTHLHzfiGQ9p-Ues130_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." NP89580.RAophiDz554QqpmvOZcSBy4v0ios6dTHLHzfiGQ9p-Ues130_provenance.
- NP89582.RAiD_b_5R_xoWoPJUHTWm_QYsoJJ6wtQZKydk50OZAddM130_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." NP89582.RAiD_b_5R_xoWoPJUHTWm_QYsoJJ6wtQZKydk50OZAddM130_provenance.
- NP89588.RAmLVDGoXsbRH3gt6AKKs0rPz9dWdvbmdhShwYtP_vytI130_assertion description "[Linkage of schizophrenia with TPH2 and 5-HTR2A gene polymorphisms in the Malay population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89588.RAmLVDGoXsbRH3gt6AKKs0rPz9dWdvbmdhShwYtP_vytI130_provenance.
- NP89592.RAg7jcK0AHox_Ohqi-4l--JJYseuKo6AhqfsbVS8ksGf4130_assertion description "[Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89592.RAg7jcK0AHox_Ohqi-4l--JJYseuKo6AhqfsbVS8ksGf4130_provenance.
- NP89594.RAvHOH0kmuE_meiVqDec6cU-SwolCxtKwhrLd0ys_W_m4130_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." NP89594.RAvHOH0kmuE_meiVqDec6cU-SwolCxtKwhrLd0ys_W_m4130_provenance.
- NP89598.RAgeJnj3D2LH9bfxhSjopz5cnOlkBtiDPCkJUIkzRKmCM130_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." NP89598.RAgeJnj3D2LH9bfxhSjopz5cnOlkBtiDPCkJUIkzRKmCM130_provenance.
- NP89601.RAhdxM2xBVlKCDQqsOYYJolZa_7-49Twa--l4AbQ00Jww130_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." NP89601.RAhdxM2xBVlKCDQqsOYYJolZa_7-49Twa--l4AbQ00Jww130_provenance.
- NP89603.RAsPmTZeDGrS6TDNtAm9bgi1yag1vdWoduC6cYLxCeG6o130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89603.RAsPmTZeDGrS6TDNtAm9bgi1yag1vdWoduC6cYLxCeG6o130_provenance.
- NP89610.RAjqjGgbKs-1uT2Jz1VTmvLytEu4OVODcAWsDvcA_Yxis130_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." NP89610.RAjqjGgbKs-1uT2Jz1VTmvLytEu4OVODcAWsDvcA_Yxis130_provenance.
- NP89618.RApvoshczbnQLIluh3WG-LgSCvKSxWXTILV0WG9PkGRDo130_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." NP89618.RApvoshczbnQLIluh3WG-LgSCvKSxWXTILV0WG9PkGRDo130_provenance.
- NP89623.RAkmJHfrj3MioLnPkW0mB5gB_nNim6sIh0ee6uJsJCoDk130_assertion description "[Inherited genetic variant predisposes to aggressive but not indolent prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89623.RAkmJHfrj3MioLnPkW0mB5gB_nNim6sIh0ee6uJsJCoDk130_provenance.
- NP89627.RAsiZ_TJu3OYbeezpW9ODUb-ywSsRV5lZ_nSSs9xge3Ng130_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." NP89627.RAsiZ_TJu3OYbeezpW9ODUb-ywSsRV5lZ_nSSs9xge3Ng130_provenance.
- NP89631.RAjmREs1SFMj2l75eafjvgU0cMg3a2AzhcAT-P9QK1Ikk130_assertion description "[from these analyses indicated that variance in the activity of neurochemical pathways implicated in neurodegeneration is explained, at least in part, by the inheritance of common genetic polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89631.RAjmREs1SFMj2l75eafjvgU0cMg3a2AzhcAT-P9QK1Ikk130_provenance.
- NP89632.RAhcO0z_g7MyKt2TPuN7mGPurFgEbSeHloztAkID6pFiI130_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." NP89632.RAhcO0z_g7MyKt2TPuN7mGPurFgEbSeHloztAkID6pFiI130_provenance.
- NP89633.RAjhbxvQ6sybBBO3UfrZxG0miougaFEEXKVGCV29UuZ4E130_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." NP89633.RAjhbxvQ6sybBBO3UfrZxG0miougaFEEXKVGCV29UuZ4E130_provenance.
- NP89634.RAoV-Kq4FxrNHNDcQwjWVN0v--JmJR3GUeN-1xXBYveH0130_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." NP89634.RAoV-Kq4FxrNHNDcQwjWVN0v--JmJR3GUeN-1xXBYveH0130_provenance.
- NP89636.RAmPRXbBo7uPA30lwaS-FvmBj7oUK7VSpJXA3uAE8xT3U130_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." NP89636.RAmPRXbBo7uPA30lwaS-FvmBj7oUK7VSpJXA3uAE8xT3U130_provenance.
- NP89637.RAmgRlDL22A36dVFEg2xHfTsnWxNCLhpEO1gCWpkIVExk130_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." NP89637.RAmgRlDL22A36dVFEg2xHfTsnWxNCLhpEO1gCWpkIVExk130_provenance.
- NP89638.RAm7c1PsTrxAbtA4aUSIB0x_ehXPwsZh_mrKjlkxHwdlk130_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." NP89638.RAm7c1PsTrxAbtA4aUSIB0x_ehXPwsZh_mrKjlkxHwdlk130_provenance.
- NP89641.RAsCyXJdvALhLhwrfF1kudWg4-TkUQXvbjknYoNzRKXiU130_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." NP89641.RAsCyXJdvALhLhwrfF1kudWg4-TkUQXvbjknYoNzRKXiU130_provenance.
- NP89644.RAlVjHzB3Tii8B22K0Qof1_mVCy-Te-u8uG0V62DlEPcg130_assertion description "[Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89644.RAlVjHzB3Tii8B22K0Qof1_mVCy-Te-u8uG0V62DlEPcg130_provenance.
- NP89659.RAhU5pcH0bBmVXnm9czUTAW8FNVMwXbRDh6tL62UAFWIU130_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." NP89659.RAhU5pcH0bBmVXnm9czUTAW8FNVMwXbRDh6tL62UAFWIU130_provenance.
- NP89666.RAv8L0d9uWyE-gyJeMv_7pDIoPz-QsUDQr-VuuPtX8tQc130_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." NP89666.RAv8L0d9uWyE-gyJeMv_7pDIoPz-QsUDQr-VuuPtX8tQc130_provenance.
- NP89667.RAoR0aW3PR_2RoVNjeChvxbgxxat4yEHu6o7u65pAjHuw130_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." NP89667.RAoR0aW3PR_2RoVNjeChvxbgxxat4yEHu6o7u65pAjHuw130_provenance.
- NP89669.RAuB3xnPRhK_VS8d1Ha9W3PDljScKnBmsWCVW6p-HUX3I130_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." NP89669.RAuB3xnPRhK_VS8d1Ha9W3PDljScKnBmsWCVW6p-HUX3I130_provenance.
- NP89672.RAm9d_IQqAtUENaME-afOgF04VdtheVsDea2l5Ck8V9KA130_assertion description "[In this study the effects of KCNQ1 and AP3S1 variants on susceptibility to T2D in the Chinese Northern Han population were confirmed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89672.RAm9d_IQqAtUENaME-afOgF04VdtheVsDea2l5Ck8V9KA130_provenance.
- NP89673.RAnKuJmrcp3ZvrVwycmM0TikoZAySpHGCqEAQxuDzbYx8130_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." NP89673.RAnKuJmrcp3ZvrVwycmM0TikoZAySpHGCqEAQxuDzbYx8130_provenance.
- NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89677.RAmGDFIvyv9to7psQ2ZJf9VQOqunR4Rq2nPOiYftcEPVo130_provenance.
- NP89678.RAt-I8W66YHGokqbwJeOPZscpXHZT9qiN60mffXLLCixU130_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." NP89678.RAt-I8W66YHGokqbwJeOPZscpXHZT9qiN60mffXLLCixU130_provenance.
- NP89690.RAq0DGYcoQz6hR-eqfOsuL6HFc16DyHh1A6RisFtd_T_U130_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." NP89690.RAq0DGYcoQz6hR-eqfOsuL6HFc16DyHh1A6RisFtd_T_U130_provenance.
- NP89699.RAt_dfno6nPztVYGuldK-9T6wDELuGYhZW1YrJpXZgq9I130_assertion description "[Association of polymorphisms of ABCA1 and ROS1 with hypertension in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89699.RAt_dfno6nPztVYGuldK-9T6wDELuGYhZW1YrJpXZgq9I130_provenance.
- NP89700.RAjDV9ISnWrnY9jGMIMSYbQkeW0gYa3owaTwc_Nk8lwx0130_assertion description "[Association of common JAK2 variants with body fat, insulin sensitivity and lipid profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89700.RAjDV9ISnWrnY9jGMIMSYbQkeW0gYa3owaTwc_Nk8lwx0130_provenance.
- NP89712.RAuzQCFyRy-8ZPUyf3m1MNS064O2RFCR32vGg8oFU5hI0130_assertion description "[Quinone oxidoreductase (NQO1) gene polymorphism may not confer a susceptibility to mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89712.RAuzQCFyRy-8ZPUyf3m1MNS064O2RFCR32vGg8oFU5hI0130_provenance.
- NP89714.RApJaLqoLtAXaXVSRIe9F_HmZNkOwVhbhwYJCuXYp2Lgk130_assertion description "[Adverse birth outcomes associated with maternal smoking and polymorphisms in the N-Nitrosamine-metabolizing enzyme genes NQO1 and CYP2E1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89714.RApJaLqoLtAXaXVSRIe9F_HmZNkOwVhbhwYJCuXYp2Lgk130_provenance.
- NP89717.RAjTo0Z9lpd9n8fW_Hsq4EWn4rEBJQEpcHa5kWwUGLQDM130_assertion description "[beta2-Adrenergic receptor genotype and preterm delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89717.RAjTo0Z9lpd9n8fW_Hsq4EWn4rEBJQEpcHa5kWwUGLQDM130_provenance.
- NP89718.RAghO_b-7vk8r-Ob8NHj_9MKIYogrjF1aA6z-yxAtV3OU130_assertion description "[beta2 adrenoceptor gene polymorphisms in cystic fibrosis lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89718.RAghO_b-7vk8r-Ob8NHj_9MKIYogrjF1aA6z-yxAtV3OU130_provenance.
- NP89723.RAsBlhIfd-KBg14cNWalGM_dGkSnWz7SY582_I4-_EVX0130_assertion description "[, the Glu27 allele of the ADRB2 gene may confer increased risk of autism and shows increased strength with exposure to pregnancy related stress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89723.RAsBlhIfd-KBg14cNWalGM_dGkSnWz7SY582_I4-_EVX0130_provenance.
- NP89732.RAhksijrQVsyfuXGnSMO2_gcSQU359LzRyyfDEisPEQds130_assertion description "[Association between beta2 adrenergic receptor polymorphisms and rheumatoid arthritis in conjunction with human leukocyte antigen (HLA)-DRB1 shared epitope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89732.RAhksijrQVsyfuXGnSMO2_gcSQU359LzRyyfDEisPEQds130_provenance.
- NP89737.RAtDzeKy2qXnQGxVMaKrSAQv0nOHGf7Y2YpUYsNa0nwkE130_assertion description "[Ser49Gly and haplotype combinations of Ser49Gly and Gly389Arg of the beta(1)AR gene are associated with aerobic power, but not with the response to physical training in patients with CAD included in the CAREGENE study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89737.RAtDzeKy2qXnQGxVMaKrSAQv0nOHGf7Y2YpUYsNa0nwkE130_provenance.
- NP89745.RAsPQzemJvf1uS7J7KK5uoUUrzyM9DS6agZgNgHD4Ef30130_assertion description "[Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89745.RAsPQzemJvf1uS7J7KK5uoUUrzyM9DS6agZgNgHD4Ef30130_provenance.
- NP89752.RAj4psf4bkGBYFxY0XpM_vlOIygGbcLxkNCj9kBm5ydPg130_assertion description "[Low potentiality of angiotensin-converting enzyme gene insertion/deletion polymorphism as a useful predictive marker for carotid atherogenesis in a large general population of a Japanese city: the Suita study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89752.RAj4psf4bkGBYFxY0XpM_vlOIygGbcLxkNCj9kBm5ydPg130_provenance.
- NP89753.RAuphSDBFSkOIDBXZA5oTk6CTKQlCd4_Yf3s6Auvt7WLQ130_assertion description "[Thirty-nine patients with Wegener's granulomatosis were genotyped for the deletion/insertion polymorphism in intron 16 of the ACE gene, a biallelic polymorphism in codon 25 of the TGF-beta1 gene and a biallelic polymorphism at position -1082 of the IL-10 gene and compared with healthy blood donors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89753.RAuphSDBFSkOIDBXZA5oTk6CTKQlCd4_Yf3s6Auvt7WLQ130_provenance.
- NP89754.RAmPeHU4abjZiPx8mAnuwC3zzf1vVmixeyLx6Mey3j_QY130_assertion description "[The ACE D allele is an independent risk factor for pneumonia in elderly persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89754.RAmPeHU4abjZiPx8mAnuwC3zzf1vVmixeyLx6Mey3j_QY130_provenance.
- NP89756.RAuGtqF72Ury5oZ0FsTrCn0ypFj0O5bWoLIfvqO2Mkp94130_assertion description "[To study the association between ACE genotype and risk of pneumonia, the distribution of the ACE I/D polymorphism was compared with healthy control subjects from the same geographic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89756.RAuGtqF72Ury5oZ0FsTrCn0ypFj0O5bWoLIfvqO2Mkp94130_provenance.
- NP89760.RAks6WMfCMsfa-oR1Uk5ZqFdfrlJROB3DreEGt-UDuUaU130_assertion description "[ACE polymorphisms are associated with ISR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89760.RAks6WMfCMsfa-oR1Uk5ZqFdfrlJROB3DreEGt-UDuUaU130_provenance.
- NP89761.RAtazE86nLo-qNuJvpJdpUCwlUZT4SEpi4Z0SPQzQn8dU130_assertion description "[Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene and arterial oxygen saturation at high altitude.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89761.RAtazE86nLo-qNuJvpJdpUCwlUZT4SEpi4Z0SPQzQn8dU130_provenance.
- NP89765.RAtpL0tAfpjNM8UC9_D3o5JF_fYCKWyXT9Co0fG6_6F1I130_assertion description "[Is angiotensin I-converting enzyme a `master` disease gene?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89765.RAtpL0tAfpjNM8UC9_D3o5JF_fYCKWyXT9Co0fG6_6F1I130_provenance.
- NP89775.RApk13eou4k21M8yOm6_W2UTGbWSp_qSwu-1WoITjk9cc130_assertion description "[Angiotension-converting enzyme gene I/D polymorphism in patients with angina and normal coronary arteriograms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89775.RApk13eou4k21M8yOm6_W2UTGbWSp_qSwu-1WoITjk9cc130_provenance.
- NP89778.RAnLKMbm0HTF87IUO4M5G2wTYcpkCAW77b5MNscRNL2Vc130_assertion description "[Based on reports indicating a role for angiotensin-converting enzyme (ACE) in the pathogenesis of intracranial aneurysms (IAs) as well as hypertension, an independent risk factor for IAs, the authors investigated the association between an insertion/deletion (I/D) polymorphism in the ACE gene and IAs in a Caucasian population in the US.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89778.RAnLKMbm0HTF87IUO4M5G2wTYcpkCAW77b5MNscRNL2Vc130_provenance.
- NP89782.RAgHkUD0A8IXxr8RC_8O7x8OQ1Eh6XayXO4GGonU-y1P4130_assertion description "[Association between angiotensin-converting enzyme gene polymorphism and childhood allergic rhinitis in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89782.RAgHkUD0A8IXxr8RC_8O7x8OQ1Eh6XayXO4GGonU-y1P4130_provenance.
- NP89783.RAh2MakotxfrXj6orKVxxj5QspqzzJf6YDtvEHJ8LRk5I130_assertion description "[Angiotensin-converting enzyme (ACE) activity is increased in blood and cerebrospinal fluid of patients with multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89783.RAh2MakotxfrXj6orKVxxj5QspqzzJf6YDtvEHJ8LRk5I130_provenance.
- NP89785.RApl4vSArp0gm2OkkSmY3xdRQtMxdt6bWiuqkMEcM2O_I130_assertion description "[D-allele of ACE polymorphism is associated with increased magnitude of QT dispersion prolongation in elderly Chinese: 4-year follow-up study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89785.RApl4vSArp0gm2OkkSmY3xdRQtMxdt6bWiuqkMEcM2O_I130_provenance.
- NP89787.RAmF6A2gqtdiUht7hx_sG7O8pOspJaxCwaMKBCrRQ7stE130_assertion description "[The prevalence of the homozygous ACE II genotype was significantly higher in patients with early-onset psoriasis than among control subjects (30.9% vs 19.2%, P = 0.016), yielding an odds ratio of 1.88 95% confidence interval (CI): 1.12-3.15 for early-onset disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89787.RAmF6A2gqtdiUht7hx_sG7O8pOspJaxCwaMKBCrRQ7stE130_provenance.
- NP89788.RAhHafzt2gTQ78ldcpe1heBxW1DO9sXc653id9AACereY130_assertion description "[The I allele of the ACE gene is associated with a higher functional capacity in female patients, and might partly explain the individual variability in the phenotypic manifestation of McArdle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89788.RAhHafzt2gTQ78ldcpe1heBxW1DO9sXc653id9AACereY130_provenance.
- NP89794.RAshiVPLpnleuxmDD6oIJRlWQrOnG6b-05ke-CtDGC6hU130_assertion description "[Although none of the single gene polymorphisms of the RAS affected renal allograft function, combinations of these genotypes were associated with the outcome of allograft function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89794.RAshiVPLpnleuxmDD6oIJRlWQrOnG6b-05ke-CtDGC6hU130_provenance.
- NP89796.RAk1tm8kqhXQMz46CeBs65o_Eivx0zIC_LhManwc3Lrxc130_assertion description "[No relation between angiotensin-converting enzyme gene polymorphism and pseudoexfoliation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89796.RAk1tm8kqhXQMz46CeBs65o_Eivx0zIC_LhManwc3Lrxc130_provenance.
- NP89805.RAua_0NRD1ZSkCAs3dgUeCU5AZy4canxJxUgLdywg9DtQ130_assertion description "[Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89805.RAua_0NRD1ZSkCAs3dgUeCU5AZy4canxJxUgLdywg9DtQ130_provenance.
- NP89806.RApOaGZPlAQUXvFroTBILLjavUcjEBedIsYxWucsgmPqQ130_assertion description "[Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89806.RApOaGZPlAQUXvFroTBILLjavUcjEBedIsYxWucsgmPqQ130_provenance.
- NP89807.RAjYeHM5dS62LlglJqDGPfbQ2qfh0clwlu0fW-m-trviY130_assertion description "[Association of DAO and G72(DAOA)/G30 genes with bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89807.RAjYeHM5dS62LlglJqDGPfbQ2qfh0clwlu0fW-m-trviY130_provenance.
- NP89809.RAl4-2GpL-oWk5uvtH5DgSzcrS8gQH6ZRhjAQS042ubXM130_assertion description "[The aim of this study was to verify the finding that CYP7A1 polymorphism may be associated with gallstone disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89809.RAl4-2GpL-oWk5uvtH5DgSzcrS8gQH6ZRhjAQS042ubXM130_provenance.
- NP89810.RAnMO1I6AJs04fbaUPavn4F3dyIQSGiFn0SKvVpYX6HNA130_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." NP89810.RAnMO1I6AJs04fbaUPavn4F3dyIQSGiFn0SKvVpYX6HNA130_provenance.
- NP89815.RAtSxgpL7hBse4bEFMY9uc3rJVbJrBECkk2_tNVJgxXgk130_assertion description "[Association of a polymorphism of CYP3A4 with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89815.RAtSxgpL7hBse4bEFMY9uc3rJVbJrBECkk2_tNVJgxXgk130_provenance.
- NP89816.RAkqZS8GlVUW0UBket0U4v5jXL6UR85jV2eS-RcsBzQKA130_assertion description "[APOA5, LDLR, CYP3A4 and C1QTNF5 are susceptibility loci for metabolic syndrome in Japanese people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89816.RAkqZS8GlVUW0UBket0U4v5jXL6UR85jV2eS-RcsBzQKA130_provenance.
- NP89822.RAvzZ716JKJMGloRdrWr_9CNdlD67xcCgW2Xeb-Kjy1T8130_assertion description "[Elucidation of CYP2E1 5' regulatory RsaI/Pstl allelic variants and their role in risk for oral cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89822.RAvzZ716JKJMGloRdrWr_9CNdlD67xcCgW2Xeb-Kjy1T8130_provenance.
- NP89829.RApHyCoqpnt0gf9HXzGRhd1FdiW3DjdAXu6xNSQU7g-3w130_assertion description "[Genetic differences in ethanol metabolizing enzymes and blood pressure in Japanese alcohol consumers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89829.RApHyCoqpnt0gf9HXzGRhd1FdiW3DjdAXu6xNSQU7g-3w130_provenance.
- NP89830.RAo93gbSPNg3Vkr8UOOq4TzzFp6LcpbV5RGkobqAriWO8130_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." NP89830.RAo93gbSPNg3Vkr8UOOq4TzzFp6LcpbV5RGkobqAriWO8130_provenance.
- NP89842.RAh6gCbUREdoajsnhGdIbRiKL1UB4-ba1cga2PQwyLIyw130_assertion description "[Cytochrome P-450 2D6*10 C188T polymorphism is associated with antipsychotic-induced persistent tardive dyskinesia in Chinese schizophrenic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89842.RAh6gCbUREdoajsnhGdIbRiKL1UB4-ba1cga2PQwyLIyw130_provenance.
- NP89844.RAksIVm5KqX9VBNslRjufA1cumCs8cd1jS1A_WCkFvBU0130_assertion description "[The efficacy of simvastatin is not influenced by CYP2D6 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89844.RAksIVm5KqX9VBNslRjufA1cumCs8cd1jS1A_WCkFvBU0130_provenance.
- NP89847.RAs7LTqyuc1haBYdemj59wR-9uzlJ2NFg5psoTVe_hKvs130_assertion description "[Prevention of postoperative nausea and vomiting with granisetron and dolasetron in relation to CYP2D6 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89847.RAs7LTqyuc1haBYdemj59wR-9uzlJ2NFg5psoTVe_hKvs130_provenance.
- NP89849.RApoNzSUqZqZcRjxEA3PLz64UDm7AHjZElQYQBCK1qRpQ130_assertion description "[Our findings suggest that the CYP2D6*5 allele is likely to affect vulnerability to development of NMS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89849.RApoNzSUqZqZcRjxEA3PLz64UDm7AHjZElQYQBCK1qRpQ130_provenance.
- NP89852.RAgdWOOwVaHyOJ4LjnGs-3Y-2KlYpMbtcs2nQi6RIhTlw130_assertion description "[Role of CYP2C9 and CYP2C19 polymorphisms in patients with atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89852.RAgdWOOwVaHyOJ4LjnGs-3Y-2KlYpMbtcs2nQi6RIhTlw130_provenance.
- NP89856.RApiUMqQLPQO_xa8REtDt-d2hl1YneQJbnlDbi6VkO4dQ130_assertion description "[Biological effect of increased maintenance dose of clopidogrel in cardiovascular outpatients and influence of the cytochrome P450 2C19*2 allele on clopidogrel responsiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89856.RApiUMqQLPQO_xa8REtDt-d2hl1YneQJbnlDbi6VkO4dQ130_provenance.
- NP89862.RAmVoNkip9Hzmr3cT7h9VKIggqoDTSrrlzUIqtBRfkAbk130_assertion description "[Interactions between genotype and retrospective ADHD symptoms predict lifetime smoking risk in a sample of young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89862.RAmVoNkip9Hzmr3cT7h9VKIggqoDTSrrlzUIqtBRfkAbk130_provenance.
- NP89869.RAtSr3HtEJMUAXc1zCQ8xI5iT3DtJwiBtDX0g0S7XJN90130_assertion description "[The present data do not suggest a relevant association between CYP1A1 polymorphisms and focal nodular hyperplasia of the liver in female Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89869.RAtSr3HtEJMUAXc1zCQ8xI5iT3DtJwiBtDX0g0S7XJN90130_provenance.
- NP89890.RAh0TUF2tHzJ0DeCPHi6_nobZ0Q0DZ0psVksvGQ6QPvro130_assertion description "[Moderate drinkers who are homozygous for the slow-oxidizing ADH3 allele have higher HDL levels and a substantially decreased risk of myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89890.RAh0TUF2tHzJ0DeCPHi6_nobZ0Q0DZ0psVksvGQ6QPvro130_provenance.
- NP89892.RApPU9tz7L7qdld3FDc6mZ8GLbZiWItrH77WHjCE9JWMw130_assertion description "[These data suggest that the presence of the CYP2E1 intron 6 DD genotype might confer a higher risk of alcoholic CP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89892.RApPU9tz7L7qdld3FDc6mZ8GLbZiWItrH77WHjCE9JWMw130_provenance.
- NP89894.RAukECsZEsbKosvyFXWyF-xPITUPXlKEPkIwUl7pgHxbc130_assertion description "[Genetic variation in alcohol dehydrogenase 1C and the beneficial effect of alcohol intake on coronary heart disease risk in the Second Northwick Park Heart Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89894.RAukECsZEsbKosvyFXWyF-xPITUPXlKEPkIwUl7pgHxbc130_provenance.
- NP89895.RAiNRCppiyg9tCPqx9tIZPd3nwSswE4j8RpdIWgSKteFo130_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." NP89895.RAiNRCppiyg9tCPqx9tIZPd3nwSswE4j8RpdIWgSKteFo130_provenance.
- NP89899.RAicnhUTXcPfVSnfzDpBltSWRfFxax_0ZybtWn0W7Cvr4130_assertion description "[Genetic differences in ethanol metabolizing enzymes and blood pressure in Japanese alcohol consumers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89899.RAicnhUTXcPfVSnfzDpBltSWRfFxax_0ZybtWn0W7Cvr4130_provenance.
- NP89900.RAjyGAXQGWUz1Morn3osb1h7VfEGqhNrZb-Vcj2cq3S00130_assertion description "[Do the ethanol metabolizing enzymes modify the relationship between alcohol consumption and blood pressure?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89900.RAjyGAXQGWUz1Morn3osb1h7VfEGqhNrZb-Vcj2cq3S00130_provenance.
- NP89904.RAgQpqq4DIJ2Ujf1BGRiPqlz-i-MiPd7TZH9w3mvmGmLE130_assertion description "[To investigate the possible association between alcohol dehydrogenase 1B, beta-polypeptide (ADH2) genotype and allelic variants and the risk for developing essential tremor (ET).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89904.RAgQpqq4DIJ2Ujf1BGRiPqlz-i-MiPd7TZH9w3mvmGmLE130_provenance.
- NP89910.RAs4XUzkwB4iwJsCOwbgRJAsG8F6c-9sDbGtJDdehE3TY130_assertion description "[Reprimo 824 G>C and p53R2 4696 C>G single nucleotide polymorphisms and colorectal cancer: a case-control disease association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89910.RAs4XUzkwB4iwJsCOwbgRJAsG8F6c-9sDbGtJDdehE3TY130_provenance.
- NP89920.RAoiOTL0Ep9COsACrxjKfI5_Q1H0RtiWStZrC3OBrNf9o130_assertion description "[Evidence for association of chromosome 10 open reading frame (C10orf27) gene polymorphisms and multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89920.RAoiOTL0Ep9COsACrxjKfI5_Q1H0RtiWStZrC3OBrNf9o130_provenance.
- NP89921.RAs-C03jN4rWuJz_E6C-DFupEFq-13nN-b3G7JBOowEEs130_assertion description "[Polymorphisms in genes involved in innate immunity predispose toward mycetoma susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89921.RAs-C03jN4rWuJz_E6C-DFupEFq-13nN-b3G7JBOowEEs130_provenance.
- NP89924.RAiZQfYw-rnVXZmZ53X9qT3QUylGhgMYESlmne9Z7PvxI130_assertion description "[KLF6 IVS1 -27G/A polymorphism with susceptibility to gastric cancers in Korean.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89924.RAiZQfYw-rnVXZmZ53X9qT3QUylGhgMYESlmne9Z7PvxI130_provenance.
- NP89930.RApIUUr4oWHzdsvzrgK1FbMHLj6llKbvR5uismHh7iWrQ130_assertion description "[An experimental study of catechol-o-methyltransferase Val158Met moderation of delta-9-tetrahydrocannabinol-induced effects on psychosis and cognition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89930.RApIUUr4oWHzdsvzrgK1FbMHLj6llKbvR5uismHh7iWrQ130_provenance.
- NP89931.RArZErXIBHdR7nU_hQf8mtqpUmYCi8C9VucNel26GNp_E130_assertion description "[Impact of multiple genetic polymorphisms on effects of a 4-week blueberry juice intervention on ex vivo induced lymphocytic DNA damage in human volunteers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89931.RArZErXIBHdR7nU_hQf8mtqpUmYCi8C9VucNel26GNp_E130_provenance.
- NP89935.RAkrBUsTZaXhcWIPqyBJqAyvOftnwskl1cj9VU8TKq9so130_assertion description "[Antipsychotic-induced tardive dyskinesia and polymorphic variations in COMT, DRD2, CYP1A2 and MnSOD genes: a meta-analysis of pharmacogenetic interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89935.RAkrBUsTZaXhcWIPqyBJqAyvOftnwskl1cj9VU8TKq9so130_provenance.
- NP89939.RAhdo7_v1r6si9gd1HPYgrG3vDnjlSFTA3mh8ULFxC-AI130_assertion description "[Genetic variation including nonsynonymous polymorphisms of a major aggrecanase, ADAMTS-5, in susceptibility to osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89939.RAhdo7_v1r6si9gd1HPYgrG3vDnjlSFTA3mh8ULFxC-AI130_provenance.
- NP89944.RAvGMpxPpkohffBLUS91RyG6Mw3LMWddxY459TjsrVKbE130_assertion description "[Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89944.RAvGMpxPpkohffBLUS91RyG6Mw3LMWddxY459TjsrVKbE130_provenance.
- NP89945.RAoZ68vabUQ25vDSTougZlsRx8c-ZCeYjoWUMJpGeEpeU130_assertion description "[The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89945.RAoZ68vabUQ25vDSTougZlsRx8c-ZCeYjoWUMJpGeEpeU130_provenance.
- NP89947.RAlHdPk1J9Yi0g7RrPqIalfBFsM853AHx3lI7EbSVCG1s130_assertion description "[In this study we tested the hypothesis that genetic variants of CB2 gene might be associated with depression in a human population and that alteration in CB2 gene expression may be involved in the effects of abused substances including opiates, cocaine and ethanol in rodents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89947.RAlHdPk1J9Yi0g7RrPqIalfBFsM853AHx3lI7EbSVCG1s130_provenance.
- NP89955.RApiE6F9GnQ7S2rZqPMRWppAxA1xnvPrJRT650tYcXEF4130_assertion description "[Investigation of 3111T/C polymorphism of the CLOCK gene in obese individuals with or without binge eating disorder: association with higher body mass index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89955.RApiE6F9GnQ7S2rZqPMRWppAxA1xnvPrJRT650tYcXEF4130_provenance.
- NP89956.RAsX1nnao-zGY7s2bsx0GYR9l7FNmOX2MhUgoZUF1zwU8130_assertion description "[These findings suggest that the Clock gene CGC haplotype may be protective for the development of obesity and support the hypothesis that genetic variation in the Clock gene may play a role in the development of the metabolic syndrome, type 2 diabetes and cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89956.RAsX1nnao-zGY7s2bsx0GYR9l7FNmOX2MhUgoZUF1zwU8130_provenance.