Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP92213.RAque2aezpdNoPROCq-Y2PPHPcklC_cWrtsqZSA6ZlhJ4130_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." NP92213.RAque2aezpdNoPROCq-Y2PPHPcklC_cWrtsqZSA6ZlhJ4130_provenance.
- NP92215.RAnkQgoHQxkKgPRUU1Yg4X3Qnt9sBrfD-ECrMdX_Zc76I130_assertion description "[Effects of the serotonin 1A, 2A, 2C, 3A, and 3B and serotonin transporter gene polymorphisms on the occurrence of paroxetine discontinuation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92215.RAnkQgoHQxkKgPRUU1Yg4X3Qnt9sBrfD-ECrMdX_Zc76I130_provenance.
- NP92233.RAnxG0dp2egg1RLntSaaS8qqySg5UAE4Rd10Rt_0trGM0130_assertion description "[Association analysis between polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes with cocaine dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92233.RAnxG0dp2egg1RLntSaaS8qqySg5UAE4Rd10Rt_0trGM0130_provenance.
- NP92238.RAvznR54-1Be7-_gKba_Q4frOotcYrxY1RLgp-d6HjwP8130_assertion description "[, polymorphisms in the DAT1 40 base pair (bp) VNTR genotype do not predict GH deficiency or response to GH therapy in short children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92238.RAvznR54-1Be7-_gKba_Q4frOotcYrxY1RLgp-d6HjwP8130_provenance.
- NP92239.RAon2s85NQ0REpMTWqmmez_lt1vRB1BEoQYXinlaSJuYU130_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." NP92239.RAon2s85NQ0REpMTWqmmez_lt1vRB1BEoQYXinlaSJuYU130_provenance.
- NP92244.RApvQZHNSNQLZBD7kH4saL06bBxAK1fiyvRN1ZVdJg-Hg130_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." NP92244.RApvQZHNSNQLZBD7kH4saL06bBxAK1fiyvRN1ZVdJg-Hg130_provenance.
- NP92247.RAp62OvfeaNHlhXmzOIcsDaw1uMc6hnE3nMcrAENqR71g130_assertion description "[The critical role of the solute carrier family 6 (neurotransmitter transporter, betaine/GABA) member 12 (SLC6A12) gene in GABAergic transmission, which is associated with mucus production in asthma, makes it a candidate gene for AIA association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92247.RAp62OvfeaNHlhXmzOIcsDaw1uMc6hnE3nMcrAENqR71g130_provenance.
- NP92249.RAvc8m7Wu9h0vbQRiAIDAKU7BzJ8kHhkm17oRo2IBnzM8130_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." NP92249.RAvc8m7Wu9h0vbQRiAIDAKU7BzJ8kHhkm17oRo2IBnzM8130_provenance.
- NP92251.RAqy2K9KSStmUlp7UWjKTkWDXonuXR1UiVE-sJZibFrKE130_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." NP92251.RAqy2K9KSStmUlp7UWjKTkWDXonuXR1UiVE-sJZibFrKE130_provenance.
- NP92254.RAiI8UAgdPAdkFa9u9dIrQPFcAqcs4Fo9a3Xpec6tkumw130_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." NP92254.RAiI8UAgdPAdkFa9u9dIrQPFcAqcs4Fo9a3Xpec6tkumw130_provenance.
- NP92257.RApuLTsFC2xbkCPy6krCkhS8PH4C5rqM36IttQCGPjmRY130_assertion description "[Association between GLUT9 and gout in Japanese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92257.RApuLTsFC2xbkCPy6krCkhS8PH4C5rqM36IttQCGPjmRY130_provenance.
- NP92262.RAvkKU6kZn3HsuitaIbdP-goFxBCIThZm9wTJwPc4TNgo130_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." NP92262.RAvkKU6kZn3HsuitaIbdP-goFxBCIThZm9wTJwPc4TNgo130_provenance.
- NP92264.RAlzZSP7UAwrrflLGsya12cV3RyAwJJivlgsLDRxbEEKo130_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." NP92264.RAlzZSP7UAwrrflLGsya12cV3RyAwJJivlgsLDRxbEEKo130_provenance.
- NP92270.RAtc06hlsUz53erDPpLPBU1WBjhGgqoo_TaXiTUzzBN68130_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." NP92270.RAtc06hlsUz53erDPpLPBU1WBjhGgqoo_TaXiTUzzBN68130_provenance.
- NP92274.RAuCjr6VTjVXTMLJT6w41kEY-Ljj3DQn8fqOFb1p2PahY130_assertion description "[Gemcitabine metabolic and transporter gene polymorphisms are associated with drug toxicity and efficacy in patients with locally advanced pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92274.RAuCjr6VTjVXTMLJT6w41kEY-Ljj3DQn8fqOFb1p2PahY130_provenance.
- NP92276.RAgqYrkQry1vQ5eRVvBI_kx2FJVGlcsL8-bm-2QbhvLmY130_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." NP92276.RAgqYrkQry1vQ5eRVvBI_kx2FJVGlcsL8-bm-2QbhvLmY130_provenance.
- NP92278.RAjtv6n1fdd8eIvdaVixTyBtKT7Me_1UN1QAUhw3xYkCc130_assertion description "[Approximately 30% of women with fallopian tube cancer have a mutation in BRCA1 or BRCA2. The highest frequencies of BRCA mutations were seen in women with fallopian tube cancer diagnosed under age 60, in Jewish women, in women with a family history of breast or ovarian cancer, and in women with a personal history of breast cancer. All patients diagnosed with invasive fallopian tube cancer should be considered candidates for genetic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92278.RAjtv6n1fdd8eIvdaVixTyBtKT7Me_1UN1QAUhw3xYkCc130_provenance.
- NP92285.RAieVi4tEz0YKbVUMaNItN8SAGuYBrru4gsNz5oUSMsiI130_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." NP92285.RAieVi4tEz0YKbVUMaNItN8SAGuYBrru4gsNz5oUSMsiI130_provenance.
- NP92286.RArCrUs-EjHlhxKMDbWCAIWGKdgqNkcwziWM9dqcxs36M130_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." NP92286.RArCrUs-EjHlhxKMDbWCAIWGKdgqNkcwziWM9dqcxs36M130_provenance.
- NP92292.RAlyVzz0axCIRnawnlTWh8p_AHZG4D6MYy3MCZfBeZTrk130_assertion description "[Association analysis of susceptibility candidate region on chromosome 5q31 for tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92292.RAlyVzz0axCIRnawnlTWh8p_AHZG4D6MYy3MCZfBeZTrk130_provenance.
- NP92293.RAkEPBD2QdTeQDuOTRU-Z1BcNkeyullKw2SeVvXv-nLpE130_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." NP92293.RAkEPBD2QdTeQDuOTRU-Z1BcNkeyullKw2SeVvXv-nLpE130_provenance.
- NP92297.RApCLepan9hCP4_Zqur-ROaeDkAuROllqSUhzcd5yjDDk130_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." NP92297.RApCLepan9hCP4_Zqur-ROaeDkAuROllqSUhzcd5yjDDk130_provenance.
- NP92298.RAu3YbDSfFrOFid1y6A1L3WAzKDvbYYAw8qO7KJ0rmXWs130_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." NP92298.RAu3YbDSfFrOFid1y6A1L3WAzKDvbYYAw8qO7KJ0rmXWs130_provenance.
- NP92302.RArbBaXQ-2MtHngD0-I8VknVUtpPwK6vDofdlTPGYs2Xg130_assertion description "[In this study, we evaluated rifampin pharmacokinetics in relation to tuberculosis, geographic region, race, and single nucleotide polymorphisms of the human transporter genes SLCO1B1, SLCO1B3, and MDR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92302.RArbBaXQ-2MtHngD0-I8VknVUtpPwK6vDofdlTPGYs2Xg130_provenance.
- NP92303.RAr6q4t786YxvOZTewrAsNgFONqWejlHRpkaxXwiLDMBo130_assertion description "[In this study, associations between IM trough concentration, clinical response and 11 single-nucleotide polymorphisms in genes involved in IM pharmacokinetics (ABCB1, ABCC2, ABCG2 CYP3A5, SLC22A1 and SLCO1B3) were investigated among 67 Japanese chronic phase CML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92303.RAr6q4t786YxvOZTewrAsNgFONqWejlHRpkaxXwiLDMBo130_provenance.
- NP92306.RAhKDDgmdkaz0yoRmcLRPhbW21UeW8EG_QAXsRvs9hPc8130_assertion description "[An intronic single nucleotide polymorphism in ABCA1 and the APOE epsilon3 allele are associated with reduced LDLc lowering by statins and identify individuals who may be resistant to maximal LDLc lowering by statins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92306.RAhKDDgmdkaz0yoRmcLRPhbW21UeW8EG_QAXsRvs9hPc8130_provenance.
- NP92322.RAqgvyE4qJCUTu5cyGL6SUPGE9G-GvwuHFGL09z8es8ME130_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." NP92322.RAqgvyE4qJCUTu5cyGL6SUPGE9G-GvwuHFGL09z8es8ME130_provenance.
- NP92325.RAmLricxk6i6teGBBru0fud4-BzCgzmVIVRYhpmoAqHLY130_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." NP92325.RAmLricxk6i6teGBBru0fud4-BzCgzmVIVRYhpmoAqHLY130_provenance.
- NP92332.RAtZHIMk2TulHSsDzOf9CnecBBzZUiEB6b-PzKf9GC_8A130_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." NP92332.RAtZHIMk2TulHSsDzOf9CnecBBzZUiEB6b-PzKf9GC_8A130_provenance.
- NP92334.RAhknoDmwaLBEB_qn6QsXVLeDY7QV66t9XrJ83fHXd9i4130_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." NP92334.RAhknoDmwaLBEB_qn6QsXVLeDY7QV66t9XrJ83fHXd9i4130_provenance.
- NP92338.RAvy636OYrAyzOfiYkaovUgbZpw6JKMqVtAGtsrSWc_lY130_assertion description "[The results have provided evidence that the HUT2 gene may play a certain role in developing MetS and its related traits in Asian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92338.RAvy636OYrAyzOfiYkaovUgbZpw6JKMqVtAGtsrSWc_lY130_provenance.
- NP92344.RAirSIokodXg52wO0rTkuUhuqWps2HmqNUYSoT8RgfuiY130_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." NP92344.RAirSIokodXg52wO0rTkuUhuqWps2HmqNUYSoT8RgfuiY130_provenance.
- NP92349.RAgdLIy28N51n484irLXGM_PKSo3NJ97BvChjIzHdtstE130_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." NP92349.RAgdLIy28N51n484irLXGM_PKSo3NJ97BvChjIzHdtstE130_provenance.
- NP92351.RAuQjEwAeqrvyZv5F4Mmq4ysOLH8Eby6Mg2DY-DXPlzi8130_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." NP92351.RAuQjEwAeqrvyZv5F4Mmq4ysOLH8Eby6Mg2DY-DXPlzi8130_provenance.
- NP92353.RArgLbq90YvBMqPHlhrK9_I1Jah6ix_6q2o3CPen2YZ9Y130_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." NP92353.RArgLbq90YvBMqPHlhrK9_I1Jah6ix_6q2o3CPen2YZ9Y130_provenance.
- NP92361.RApBLPOJhRSqA3OOaFuLnupuPNjEXI6hcBrVP03el7fWw130_assertion description "[To investigate whether polymorphisms of SIM2 gene are associated with congenital scoliosis (CS) in a Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92361.RApBLPOJhRSqA3OOaFuLnupuPNjEXI6hcBrVP03el7fWw130_provenance.
- NP92366.RAoJzouNtuucsczBVz4c6khobyRBXzMX3nicw8ykSyQ34130_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." NP92366.RAoJzouNtuucsczBVz4c6khobyRBXzMX3nicw8ykSyQ34130_provenance.
- NP92367.RAmn5ZvYr8jGOTN_tdvrWxEHjpjTqANn2205ixOTa3nwc130_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." NP92367.RAmn5ZvYr8jGOTN_tdvrWxEHjpjTqANn2205ixOTa3nwc130_provenance.
- NP92368.RAqfsmRDzW3UoQPTOGpgL1aO9oHUA0PqoU6zoWB0v8aZE130_assertion description "[A genome-wide scan for common alleles affecting risk for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92368.RAqfsmRDzW3UoQPTOGpgL1aO9oHUA0PqoU6zoWB0v8aZE130_provenance.
- NP92371.RAqm2NFPe5mq3I0E9T7jXc040KCxVs6YDQQqW8p0nOqi4130_assertion description "[This highly validated qPCR test supersedes other approaches for copy number screening of the SHOX region in terms of reliability, accuracy, and cost efficiency. In addition, another strong point is the fact that it can be easily implemented in any standard equipped molecular laboratory. Our qPCR-based test is highly recommended for molecular diagnostics of idiopathic short stature and allied disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92371.RAqm2NFPe5mq3I0E9T7jXc040KCxVs6YDQQqW8p0nOqi4130_provenance.
- NP92373.RAoAwUkXHBnt6k03SadG9eZ4s7U5ak11LITUJFyo7BcX4130_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." NP92373.RAoAwUkXHBnt6k03SadG9eZ4s7U5ak11LITUJFyo7BcX4130_provenance.
- NP92374.RAuYDlt3Miq-wi1cV5BB985o9GIf1XG4ZKeu3A2eyb1X0130_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." NP92374.RAuYDlt3Miq-wi1cV5BB985o9GIf1XG4ZKeu3A2eyb1X0130_provenance.
- NP92375.RAjFrVcM6oIyoIs0UgBWgMYR9c1nShvFQgc7zbm5U11LE130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92375.RAjFrVcM6oIyoIs0UgBWgMYR9c1nShvFQgc7zbm5U11LE130_provenance.
- NP92382.RAtLj_nSQJl1HXGM-n93ePvfy5eP6fER5KoQMPmTPBdNo130_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." NP92382.RAtLj_nSQJl1HXGM-n93ePvfy5eP6fER5KoQMPmTPBdNo130_provenance.
- NP92406.RArlawjaCJQvPXVJsSwp7M5uCebNfTFS-DARW8WjMspzA130_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." NP92406.RArlawjaCJQvPXVJsSwp7M5uCebNfTFS-DARW8WjMspzA130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_assertion description "[This study analysed 12 single-nucleotide polymorphisms (SNPs) in selenoprotein genes glutathione peroxidase 1 (GPX1), GPX4, 15 kDa selenoprotein (SEP15), selenoprotein S (SELS), selenoprotein P (SEPP1) and thioredoxin reductase 2 (TXNRD2) and in genes that code for a key protein in Se incorporation SECIS-binding protein 2 (SBP2) and in antioxidant defence superoxide dismutase 2 (SOD2) in relation to sporadic CRC incidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92421.RAnomsuaYP4PC8Fou5FwpCOXihBIEdmhIC8XYze6ehRw0130_assertion description "[The initial Chi-square test revealed that the A->G polymorphism (rs12632110) of SEMA3F was significantly (false discovery rate <0.05) associated with MI among individuals with high serum HDL-cholesterol or among those with low serum LDL-cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92421.RAnomsuaYP4PC8Fou5FwpCOXihBIEdmhIC8XYze6ehRw0130_provenance.
- NP92423.RAvlV_pdNcvjr3z75-2iHZl6dXXJZ0_ap1Lfw1e-XWQ6U130_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." NP92423.RAvlV_pdNcvjr3z75-2iHZl6dXXJZ0_ap1Lfw1e-XWQ6U130_provenance.
- NP92425.RAoEc7Ipt3GwM29QmHI2oYaww3MugTDgrlGDaZ7THw-Xg130_assertion description "[Thr715Pro P-selectin polymorphism and P-selectin release in blood obtained from the bleeding time wounds in patients with deep-vein thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92425.RAoEc7Ipt3GwM29QmHI2oYaww3MugTDgrlGDaZ7THw-Xg130_provenance.
- NP92439.RAudPp_doZIIyFHK9goYxcK7vbPOMohYgXaHvaZ7EFcpg130_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." NP92439.RAudPp_doZIIyFHK9goYxcK7vbPOMohYgXaHvaZ7EFcpg130_provenance.
- NP92440.RAjkLoTQDxTZHBfFtYjiSFVVIxQeZrQZoz68I_v4I--9g130_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." NP92440.RAjkLoTQDxTZHBfFtYjiSFVVIxQeZrQZoz68I_v4I--9g130_provenance.
- NP92447.RAv60l0G86poQlOChBaKmFIj7jmyc2Ou37T0i9kwB6AJU130_assertion description "[The polymorphisms in +801 region of CXCL12 (SDF-1) are possibly related to OBI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92447.RAv60l0G86poQlOChBaKmFIj7jmyc2Ou37T0i9kwB6AJU130_provenance.
- NP92455.RAmgGbxju-zKTOaXACGit9HA1mPoqQQmZ7FscQfCG4sXc130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92455.RAmgGbxju-zKTOaXACGit9HA1mPoqQQmZ7FscQfCG4sXc130_provenance.
- NP92469.RAuHH1IOsKE5AWAj1owMGipQAMvdEEqt8JrlPtu9xocMY130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92469.RAuHH1IOsKE5AWAj1owMGipQAMvdEEqt8JrlPtu9xocMY130_provenance.
- NP92474.RArrWtoUzjGX29rI5JWNq-kPHp9-JPd1muJb8-WRE8Mrs130_assertion description "[The enzyme-linked immunosorbent assay (ELISA) and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) were, respectively, used to measure the plasma MCP-1 level and MCP-1 polymorphism in 70 healthy controls and in 64 patients with PID before and after they received routine treatment protocols.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92474.RArrWtoUzjGX29rI5JWNq-kPHp9-JPd1muJb8-WRE8Mrs130_provenance.
- NP92476.RAvCgoEn1NvFoPuR4NQT9YGs8TNuuRsDqiOQR9JqQiR_w130_assertion description "[This study aimed to investigate the association between MCP1 -2518 polymorphisms and COPD and between this polymorphism and plasma MCP-1 levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92476.RAvCgoEn1NvFoPuR4NQT9YGs8TNuuRsDqiOQR9JqQiR_w130_provenance.
- NP92486.RAkJ_hVglZXWHLLs1Mj8xiLeLT2VwDjNhAjj1i6h_byi4130_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." NP92486.RAkJ_hVglZXWHLLs1Mj8xiLeLT2VwDjNhAjj1i6h_byi4130_provenance.
- NP92489.RAj-6Q36LV2p-rqb-kOrgFOrnnTDI5fPu8-lDvkpVxlmQ130_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." NP92489.RAj-6Q36LV2p-rqb-kOrgFOrnnTDI5fPu8-lDvkpVxlmQ130_provenance.
- NP92491.RAqxJyP60qu1P4sR2mSqX5PMrH42I5GEZWNqI5iEImaxw130_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." NP92491.RAqxJyP60qu1P4sR2mSqX5PMrH42I5GEZWNqI5iEImaxw130_provenance.
- NP92494.RAgvXHLHkT2XdLgCisPvpDWnXw2Ax4rkCZ2T698OPjVRE130_assertion description "[We aimed to study whether mutations in the beta-subunits of sodium channel (SCN1B and SCN2B) would also be associated with abnormal cardiac excitation in BrS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92494.RAgvXHLHkT2XdLgCisPvpDWnXw2Ax4rkCZ2T698OPjVRE130_provenance.
- NP92499.RAl9DwCb51anq8pFXeYSQy6HePrA--vfmDoyQVLCj4XgA130_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." NP92499.RAl9DwCb51anq8pFXeYSQy6HePrA--vfmDoyQVLCj4XgA130_provenance.
- NP92501.RAu8D-laZxNxEr7LQ4mIJjJiA1k51UFPQc57UxN63oJpY130_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." NP92501.RAu8D-laZxNxEr7LQ4mIJjJiA1k51UFPQc57UxN63oJpY130_provenance.
- NP92504.RAtMo1oBJKXlQEadB9gerCljcEPM7JVl5_HiNN1XK0pmM130_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." NP92504.RAtMo1oBJKXlQEadB9gerCljcEPM7JVl5_HiNN1XK0pmM130_provenance.
- NP92514.RAqpOp3MF2Uv3CoIpUHecp7_crqLOay6zIxtJBWdkWkmA130_assertion description "[Loci associated with AD also influence neuroimaging correlates of this disease. Furthermore, neuroimaging analysis identified 2 additional loci of high interest for further study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92514.RAqpOp3MF2Uv3CoIpUHecp7_crqLOay6zIxtJBWdkWkmA130_provenance.
- NP92517.RAsM74Yb6Aw9EY4PAIKWG3Lyp4h0SiKIxNQRyCtHR-C5I130_assertion description "[Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92517.RAsM74Yb6Aw9EY4PAIKWG3Lyp4h0SiKIxNQRyCtHR-C5I130_provenance.
- NP92518.RAoDy5fRfq2g7BppEGorLLpv50891aUjDUjKg5YDWl8iA130_assertion description "[We also replicated previous associations at CR1 (rs6701713; P(M) = 4.6 10(-10), P(J) = 5.2 10(-11)), CLU (rs1532278; P(M) = 8.3 10(-8), P(J) = 1.9 10(-8)), BIN1 (rs7561528; P(M) = 4.0 10(-14), P(J) = 5.2 10(-14)) and PICALM (rs561655; P(M) = 7.0 10(-11), P(J) = 1.0 10(-10)), but not at EXOC3L2, to late-onset Alzheimer's disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92518.RAoDy5fRfq2g7BppEGorLLpv50891aUjDUjKg5YDWl8iA130_provenance.
- NP92520.RAtpnquckCUepqvFecZllIqI-W-3Bi5oVN3oIjjRKVAos130_assertion description "[Genome-wide association study of Alzheimer's disease with psychotic symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92520.RAtpnquckCUepqvFecZllIqI-W-3Bi5oVN3oIjjRKVAos130_provenance.
- NP92530.RAs3ORG_A6-lPThrBmK3jvGfU_wCyzwZ1bOLiA3agu0FE130_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." NP92530.RAs3ORG_A6-lPThrBmK3jvGfU_wCyzwZ1bOLiA3agu0FE130_provenance.
- NP92533.RAkli5tTVqJjpmb3Gq7T4xzXgYjmV2099_nkIarvYKayY130_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." NP92533.RAkli5tTVqJjpmb3Gq7T4xzXgYjmV2099_nkIarvYKayY130_provenance.
- NP92540.RAkkIsNaEIBegoWKs0X5OBnR62GWGjwGdZNPTpECWivIw130_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." NP92540.RAkkIsNaEIBegoWKs0X5OBnR62GWGjwGdZNPTpECWivIw130_provenance.
- NP92541.RAjWZ3a74WGtZCAWv7fWvSNjiJIn3u5glkUdSE7ITIWn4130_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." NP92541.RAjWZ3a74WGtZCAWv7fWvSNjiJIn3u5glkUdSE7ITIWn4130_provenance.
- NP92546.RAvNVk7rYQOVYqL-OUaGUHaG6rDuguzRtf1oy94UpWZ04130_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." NP92546.RAvNVk7rYQOVYqL-OUaGUHaG6rDuguzRtf1oy94UpWZ04130_provenance.
- NP92548.RAnnPo87GaaBHZUDh1EBKMoqQTWDmpcpiQnZUAdXEuM54130_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." NP92548.RAnnPo87GaaBHZUDh1EBKMoqQTWDmpcpiQnZUAdXEuM54130_provenance.
- NP92556.RAjWhOfps8x6f_-vzFMTmI7HNIcM01PqaYDDNPpkFTWRc130_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." NP92556.RAjWhOfps8x6f_-vzFMTmI7HNIcM01PqaYDDNPpkFTWRc130_provenance.
- NP92565.RAvVcM_frFJs1UPckXTilu9uTBVrF-qAir0ok7VfrUiyY130_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." NP92565.RAvVcM_frFJs1UPckXTilu9uTBVrF-qAir0ok7VfrUiyY130_provenance.
- NP92569.RAjXgfchrdTrtTA9kYKT2-FrpukxYHCIlN_q7B6ewWSSE130_assertion description "[Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92569.RAjXgfchrdTrtTA9kYKT2-FrpukxYHCIlN_q7B6ewWSSE130_provenance.
- NP92572.RAqpfcw6O69qJ5mHl_tuUvjltCXqJiD9jD1Aja4Bm-BX4130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92572.RAqpfcw6O69qJ5mHl_tuUvjltCXqJiD9jD1Aja4Bm-BX4130_provenance.
- NP92575.RAskYpdNDJ1OqPplVKzjvueubWSzqyjmqQpcTQhBy_bLE130_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." NP92575.RAskYpdNDJ1OqPplVKzjvueubWSzqyjmqQpcTQhBy_bLE130_provenance.
- NP92579.RAsxV_W5a_OdgvuiP9BHUvwiJ5WAXnNsRVxmHD6RAeu7E130_assertion description "[An association study between the Val66Met polymorphism of the BDNF gene and postpartum depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92579.RAsxV_W5a_OdgvuiP9BHUvwiJ5WAXnNsRVxmHD6RAeu7E130_provenance.
- NP92583.RAgwD13U3-4Qb8ZAOUwyUY7ZYFkm-5EzGQhoz1Mpc73E8130_assertion description "[Association of brain-derived neurotrophic factor (Val66Met) genetic polymorphism with methamphetamine dependence in a Malaysian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92583.RAgwD13U3-4Qb8ZAOUwyUY7ZYFkm-5EzGQhoz1Mpc73E8130_provenance.
- NP92593.RAmsRezaqv7OEwXIIGyCYlQz5luaV-RLFD-12YDTrConI130_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." NP92593.RAmsRezaqv7OEwXIIGyCYlQz5luaV-RLFD-12YDTrConI130_provenance.
- NP92600.RAoIte5vMmIkHKwUTCIRENpi1hkdQr_s0L97nFcBx3ZMg130_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." NP92600.RAoIte5vMmIkHKwUTCIRENpi1hkdQr_s0L97nFcBx3ZMg130_provenance.
- NP92601.RAlkdNynXT1hvGTfAW0Hu6izchx2MM3bvKbnkwX0sbEQ8130_assertion description "[To address this, a comprehensive analysis of single nucleotide polymorphisms (SNPs) on the nucleotide excision repair (NER) genes (ERCC2-ERCC8, RPA1-RPA3, LIG1, RAD23B, XPA, XPC) was performed in 92 chronic phase CML patients treated with imatinib upfront.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92601.RAlkdNynXT1hvGTfAW0Hu6izchx2MM3bvKbnkwX0sbEQ8130_provenance.
- NP92606.RArGGo_J5e0_8lWxptUJFNEzXdedoH9FQMWTU_pZQNIPI130_assertion description "[To address this, a comprehensive analysis of single nucleotide polymorphisms (SNPs) on the nucleotide excision repair (NER) genes (ERCC2-ERCC8, RPA1-RPA3, LIG1, RAD23B, XPA, XPC) was performed in 92 chronic phase CML patients treated with imatinib upfront.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92606.RArGGo_J5e0_8lWxptUJFNEzXdedoH9FQMWTU_pZQNIPI130_provenance.
- NP92607.RAmLA_KYfMT2YE9-vpiWotLvaZZzZcE8lniJk1W64VgDw130_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." NP92607.RAmLA_KYfMT2YE9-vpiWotLvaZZzZcE8lniJk1W64VgDw130_provenance.
- NP92617.RAus3NlC4ZkNCSgzPriB0Sfm7-W16nx_IMenCy8PKJmQc130_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." NP92617.RAus3NlC4ZkNCSgzPriB0Sfm7-W16nx_IMenCy8PKJmQc130_provenance.
- NP92618.RAqQ06Oy62ySOdd9Jz0VcRU_q2MXgtRJvj0nbvxeC6sfo130_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." NP92618.RAqQ06Oy62ySOdd9Jz0VcRU_q2MXgtRJvj0nbvxeC6sfo130_provenance.
- NP92626.RAlK9MQvlQ5EGWUxMqu-mqEcKXmrLwlPTYB-4_CqZCPNc130_assertion description "[Our analysis indicated an independent association between an ASIC3 genetic polymorphism and insulin resistance in Taiwanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92626.RAlK9MQvlQ5EGWUxMqu-mqEcKXmrLwlPTYB-4_CqZCPNc130_provenance.
- NP92636.RAjna4IxahAk0xl-_0BUC8yV9QzLMw5PI9Kra7fdGxnrk130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in autosomal recessive RP and simplex RP patients and is commercially available. High-throughput genotyping for RP is evolving into a clinically useful genetic diagnostic tool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92636.RAjna4IxahAk0xl-_0BUC8yV9QzLMw5PI9Kra7fdGxnrk130_provenance.
- NP92640.RAsAJMpkEWppLDSu1-810nQQb8cdiJ-gqAIRc9rP5h0cg130_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." NP92640.RAsAJMpkEWppLDSu1-810nQQb8cdiJ-gqAIRc9rP5h0cg130_provenance.
- NP92643.RAqjOadw6eD57IZAJ56kMpnFZB8h9RNe5BBvqrvgGG2V8130_assertion description "[The IFNG (IFN-gamma) genotype predicts cytogenetic and molecular response to imatinib therapy in chronic myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92643.RAqjOadw6eD57IZAJ56kMpnFZB8h9RNe5BBvqrvgGG2V8130_provenance.
- NP92648.RAqckiYJqf4v7-zGvZBj_DFBJMNI86m0yXK-XLjA45egc130_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." NP92648.RAqckiYJqf4v7-zGvZBj_DFBJMNI86m0yXK-XLjA45egc130_provenance.
- NP92650.RAgr47JH7HSz30Sf2iqBz0uJ5En9o5J43Y_znVBeGsRTA130_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." NP92650.RAgr47JH7HSz30Sf2iqBz0uJ5En9o5J43Y_znVBeGsRTA130_provenance.
- NP92651.RAvLCZyWG19qF-PHlkvOVOZb63_x8AcyhC-F6xHOM_F0c130_assertion description "[Interethnic differences were elucidated for several polymorphisms that might be responsible for differential serum drug levels and optimal dose requirement for efficacious treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92651.RAvLCZyWG19qF-PHlkvOVOZb63_x8AcyhC-F6xHOM_F0c130_provenance.
- NP92663.RArBcMO6OfxIYpf4zYnarR6vmTGrhU6_DY8RtuC9ynWn4130_assertion description "[The autoimmune disease-associated IL12B and IL23R polymorphisms in multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92663.RArBcMO6OfxIYpf4zYnarR6vmTGrhU6_DY8RtuC9ynWn4130_provenance.
- NP92671.RAudApDjuWFhAZ_KGM2-45KR4qPzv-LMcIxzkaIrAYFrQ130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92671.RAudApDjuWFhAZ_KGM2-45KR4qPzv-LMcIxzkaIrAYFrQ130_provenance.
- NP92672.RAnzwxTvrMTj-XCXV-e0i1cPDA-pipuD_e2Gw3smNxA_U130_assertion description "[Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92672.RAnzwxTvrMTj-XCXV-e0i1cPDA-pipuD_e2Gw3smNxA_U130_provenance.
- NP92677.RAmHIBBEWAI7zJZJZ8xKWOd6GVXNr3L0H6b67v-nPnCJg130_assertion description "[Association of an A/C single nucleotide polymorphism in programmed cell death-ligand 1 gene with Graves' disease in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92677.RAmHIBBEWAI7zJZJZ8xKWOd6GVXNr3L0H6b67v-nPnCJg130_provenance.
- NP92679.RAmlgiYlJxBXCIQddCQv7l-mx6VmYTJgtAti2T1EfQVPI130_assertion description "[We found that the HNK1 genotype, associated with high NK cell activity, might be an independent protective factor for CRC among the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92679.RAmlgiYlJxBXCIQddCQv7l-mx6VmYTJgtAti2T1EfQVPI130_provenance.
- NP92682.RAmtPcAgZMSc6Kjum-U-RHwK5AajpATlLooCz5m1NIvFs130_assertion description "[OGG1 expression and OGG1 Ser326Cys polymorphism and risk of lung cancer in a prospective study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92682.RAmtPcAgZMSc6Kjum-U-RHwK5AajpATlLooCz5m1NIvFs130_provenance.