Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP79606.RAtmsqNVw_GfR0HyidK1aXsvknnOTheInyv6uNYD-2_X4130_assertion description "[High-throughput analysis of the C4 polymorphism by a combination of MLPA and isotype-specific ELISA's.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79606.RAtmsqNVw_GfR0HyidK1aXsvknnOTheInyv6uNYD-2_X4130_provenance.
- NP79607.RAs_kHYqufTJ5Qhn2bUzXPTXTf9cJioItXIkVyf0S1SI8130_assertion description "[Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79607.RAs_kHYqufTJ5Qhn2bUzXPTXTf9cJioItXIkVyf0S1SI8130_provenance.
- NP79608.RAu2oiO-zE3HVYug34GNOvBuYXJpTlKcMbUsL8EkHs96w130_assertion description "[A genotype score based on 18 risk alleles predicted new cases of diabetes in the community but provided only a slightly better prediction of risk than knowledge of common risk factors alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79608.RAu2oiO-zE3HVYug34GNOvBuYXJpTlKcMbUsL8EkHs96w130_provenance.
- NP79609.RAhxipcNxXhjX1kGQRdHMQzRnrFo5580tH0E6HFZ7Wi3w130_assertion description "[Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79609.RAhxipcNxXhjX1kGQRdHMQzRnrFo5580tH0E6HFZ7Wi3w130_provenance.
- NP79612.RAguLSzdeUmLJJQAWDrHg70IkpYmlUf5eZJg3lugYslNU130_assertion description "[The phenotype based risk models provided greater discrimination for type 2 diabetes than did models based on 20 common independently inherited diabetes risk alleles. The addition of genotypes to phenotype based risk models produced only minimal improvement in accuracy of risk estimation assessed by recalibration and, at best, a minor net reclassification improvement. The major translational application of the currently known common, small effect genetic variants influencing susceptibility to type 2 diabetes is likely to come from the insight they provide on causes of disease and potential therapeutic targets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79612.RAguLSzdeUmLJJQAWDrHg70IkpYmlUf5eZJg3lugYslNU130_provenance.
- NP79616.RAkM98JxryX9dDSBpkIrts_wtu0ZUAbNCF1knPMFZkFaM130_assertion description "[Using data from an ongoing GWAS of pediatric BMI in our cohort, we investigated the association of pediatric BMI with 20 single nucleotide polymorphisms at 18 type 2 diabetes loci uncovered through GWAS, consisting of ADAMTS9, CDC123-CAMK1D, CDKAL1, CDKN2A/B, EXT2, FTO, HHEX-IDE, IGF2BP2, the intragenic region on 11p12, JAZF1, KCNQ1, LOC387761, MTNR1B, NOTCH2, SLC30A8, TCF7L2, THADA, and TSPAN8-LGR5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79616.RAkM98JxryX9dDSBpkIrts_wtu0ZUAbNCF1knPMFZkFaM130_provenance.
- NP79617.RAkqRKQIUDWvV9iAvdDaU9dBGM9M-Rmt74F8nc08_LI_s130_assertion description "[Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged Danes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79617.RAkqRKQIUDWvV9iAvdDaU9dBGM9M-Rmt74F8nc08_LI_s130_provenance.
- NP79621.RAjpZp2djtR6JgLiBXyHIP0hkVcrO4q5e4ZfREjUwcMcM130_assertion description "[Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79621.RAjpZp2djtR6JgLiBXyHIP0hkVcrO4q5e4ZfREjUwcMcM130_provenance.
- NP79622.RAqzNhDfOiP-NoJV6oGEEe0-UkoU-yDHNQVHOdaliH4EI130_assertion description "[The phenotype based risk models provided greater discrimination for type 2 diabetes than did models based on 20 common independently inherited diabetes risk alleles. The addition of genotypes to phenotype based risk models produced only minimal improvement in accuracy of risk estimation assessed by recalibration and, at best, a minor net reclassification improvement. The major translational application of the currently known common, small effect genetic variants influencing susceptibility to type 2 diabetes is likely to come from the insight they provide on causes of disease and potential therapeutic targets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79622.RAqzNhDfOiP-NoJV6oGEEe0-UkoU-yDHNQVHOdaliH4EI130_provenance.
- NP79625.RAsrEUsUbUOr9edi6RXOKt0sv7AmKr-2Tdjq3jTDwkLPs130_assertion description "[HIV-1 disease-influencing effects associated with ZNRD1, HCP5 and HLA-C alleles are attributable mainly to either HLA-A10 or HLA-B*57 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79625.RAsrEUsUbUOr9edi6RXOKt0sv7AmKr-2Tdjq3jTDwkLPs130_provenance.
- NP79627.RAjGYhUg_qgb5SBs0EflIWDfVrRhSR32frefqOKcqBZC8130_assertion description "[we provide evidence for a role of genetic variation in complement genes, particularly C5 and C9, and NHL risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79627.RAjGYhUg_qgb5SBs0EflIWDfVrRhSR32frefqOKcqBZC8130_provenance.
- NP79628.RAoj-AVQ1AkKmPT7fUrd1Tz5CpLhIPhihb-YAE4PfOyCg130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79628.RAoj-AVQ1AkKmPT7fUrd1Tz5CpLhIPhihb-YAE4PfOyCg130_provenance.
- NP79631.RAtJpA4kz-hUmvK7wCSQULJHhAroz_5ZM2XSwL23ap6bM130_assertion description "[Subjects were genotyped for single nucleotide polymorphisms (SNPs) from CFH, complement component 2 (C2), complement component 3 (C3), complement factor B (CFB), age-related maculopathy susceptibility (ARMS2), HtrA serine peptidase 1 (HTRA1), and apolipoprotein E (APOE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79631.RAtJpA4kz-hUmvK7wCSQULJHhAroz_5ZM2XSwL23ap6bM130_provenance.
- NP79635.RAucfk1hKgFvaN-NZg3373nr6CICDH1TwerNLj8__o5Ig130_assertion description "[Genotyping was performed for AMD risk polymorphisms associated with age-related maculopathy susceptibility 2 (ARMS2), high temperature requirement factor A1 (HTRA1), complement factor H, and complement C3, and the risk of AMD was predicted based on genotype alone or in combination with the CEP markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79635.RAucfk1hKgFvaN-NZg3373nr6CICDH1TwerNLj8__o5Ig130_provenance.
- NP79639.RAuXM1FKt-LJB6y8g6tG77qEkoz9LHt_uVeYvm02mv8_E130_assertion description "[Population stratification among Caucasian subjects from the multicentered AREDS was observed, suggesting that it should be adjusted for in future studies. The AREDS questionable control subjects can be used as control subjects in the AREDS genome-wide association study (GWAS). Smoking was an independent risk factor for advanced AMD in the AREDS subjects. There continues to be evidence that the 10q26 (age-related maculopathy susceptibility 2 gene ARMS2) locus spanning PLEKHA1-LOC387715-HTRA1 and the C3 gene may contain multiple independent genetic risks contributing to AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79639.RAuXM1FKt-LJB6y8g6tG77qEkoz9LHt_uVeYvm02mv8_E130_provenance.
- NP79640.RAtdOngaB5wfMlxQZBWi4av7MZx6YGQ81ZylC1kHPTPwY130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79640.RAtdOngaB5wfMlxQZBWi4av7MZx6YGQ81ZylC1kHPTPwY130_provenance.
- NP79641.RArSHV8RSG0HPvRyB3ZrdLURR5RlUoCGjetP22yumdx_A130_assertion description "[Genetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79641.RArSHV8RSG0HPvRyB3ZrdLURR5RlUoCGjetP22yumdx_A130_provenance.
- NP79644.RAohxoQ40VwUgq0VE5m2vKx8aGYIJSkyjhnDkBJHVAfoc130_assertion description "[Complement component 3 polymorphisms interact with polyunsaturated fatty acids to modulate risk of metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79644.RAohxoQ40VwUgq0VE5m2vKx8aGYIJSkyjhnDkBJHVAfoc130_provenance.
- NP79645.RAshyBu7r5aKi2Gy1r0bsAAwk2IT0k1e3kXHAxHLYfIuU130_assertion description "[Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79645.RAshyBu7r5aKi2Gy1r0bsAAwk2IT0k1e3kXHAxHLYfIuU130_provenance.
- NP79655.RAoN1RQfIsADexm2g0bdR0FwDh-1HIsdvbw0df0uHZrLQ130_assertion description "[High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79655.RAoN1RQfIsADexm2g0bdR0FwDh-1HIsdvbw0df0uHZrLQ130_provenance.
- NP79658.RAjQ5V8eprYyrSEailN8IJ4Zz_PVTcxmL5gn57ga1ci58130_assertion description "[The novel tumor-suppressor Mel-18 in prostate cancer: its functional polymorphism, expression and clinical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79658.RAjQ5V8eprYyrSEailN8IJ4Zz_PVTcxmL5gn57ga1ci58130_provenance.
- NP79659.RApVHMJWNYQZvTPh62vaugdX1T8FLvhWbc5kEES1NyGRo130_assertion description "[we did not observe any convincing evidence that common polymorphisms of the lamina pathway could modulate the risk of MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79659.RApVHMJWNYQZvTPh62vaugdX1T8FLvhWbc5kEES1NyGRo130_provenance.
- NP79664.RAvXUV-QHvUywhtSQtvc1q-5Kx15jn7V8lwdDmsOqwEVE130_assertion description "[Examination of association to autism of common genetic variationin genes related to dopamine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79664.RAvXUV-QHvUywhtSQtvc1q-5Kx15jn7V8lwdDmsOqwEVE130_provenance.
- NP79668.RAkWB94c29Riy-6Ume83PDBpqbEkc2EhQADn_8g95yEK8130_assertion description "[To study the associations between XRCC2 and XRCC5 single nucleotide polymorphisms (SNPs) and chemosensitivity of human lung cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79668.RAkWB94c29Riy-6Ume83PDBpqbEkc2EhQADn_8g95yEK8130_provenance.
- NP79685.RAiWvJvjF_1FNOCaXxPWfKGqFWW8fBN2j69vsGgHQs5fI130_assertion description "[Predisposition for TMPRSS2-ERG fusion in prostate cancer by variants in DNA repair genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79685.RAiWvJvjF_1FNOCaXxPWfKGqFWW8fBN2j69vsGgHQs5fI130_provenance.
- NP79692.RAh96s5ewT_ox-sHki780OoiMgcnJ3r6PQ3wrS15VjG4E130_assertion description "[Influence of genetic polymorphisms on biomarkers of exposure and genotoxic effects in styrene-exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79692.RAh96s5ewT_ox-sHki780OoiMgcnJ3r6PQ3wrS15VjG4E130_provenance.
- NP79696.RAsq4OOrsOAUiC3h2eEqckjyKD4_Pu49IMmO9IPdm-wDw130_assertion description "[hOGG1(326), XRCC1(399) and XRCC3(241) polymorphisms influence micronucleus frequencies in human lymphocytes in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79696.RAsq4OOrsOAUiC3h2eEqckjyKD4_Pu49IMmO9IPdm-wDw130_provenance.
- NP79697.RApaLS1InEeAQDf6ioFTcONmf1AYHA1LHX84veHL-ocX8130_assertion description "[Association of single nucleotide polymorphisms in SOD2, XRCC1 and XRCC3 with susceptibility for the development of adverse effects resulting from radiotherapy for prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79697.RApaLS1InEeAQDf6ioFTcONmf1AYHA1LHX84veHL-ocX8130_provenance.
- NP79699.RAtndiYi5S8fdTa1i1opvg8x8c6YLwvEjXc9baeEY3yms130_assertion description "[We hypothesized that single nucleotide polymorphisms of DNA repair genes may be a risk factor for prostate cancer (PCa) susceptibility, influencing expression of homologous recombination (XRCC3) and nonhomologous end-joining (XRCC7) genes and conferring predisposition to PCa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79699.RAtndiYi5S8fdTa1i1opvg8x8c6YLwvEjXc9baeEY3yms130_provenance.
- NP79700.RAvTtmuFwGI0OFcDF4i5ki8KzNVB4C_2OMHATkHR-N2TI130_assertion description "[RAD51(G135C), XRCC3(C241T), GSTT1, and GSTM1 genotypes were analyzed in 372 patients with AML, 226 males and 146 females, by PCR-RFLP or PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79700.RAvTtmuFwGI0OFcDF4i5ki8KzNVB4C_2OMHATkHR-N2TI130_provenance.
- NP79701.RAgHFZCiwsvYqiIkmX4rclC8IPx2_DJ-N326UmlqnJ-0Y130_assertion description "[The results of our study suggested that the XRCC3 gene TT genotype and the APE1 gene AG genotype might increase the risk of myocardial infarcts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79701.RAgHFZCiwsvYqiIkmX4rclC8IPx2_DJ-N326UmlqnJ-0Y130_provenance.
- NP79706.RApt3ZA82jQEn7dPjzhHMWTKvngsw-ImrD-ZU1kNOjC_M130_assertion description "[RAD51 and XRCC3 polymorphism frequency and risk of myelodysplastic syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79706.RApt3ZA82jQEn7dPjzhHMWTKvngsw-ImrD-ZU1kNOjC_M130_provenance.
- NP79707.RAqYr_ODZI2RGPOTgcK3VU2q_4gcmarlfPHMvxGMyusag130_assertion description "[Polymorphisms of detoxification and DNA repair enzymes in myelodyplastic syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79707.RAqYr_ODZI2RGPOTgcK3VU2q_4gcmarlfPHMvxGMyusag130_provenance.
- NP79710.RAk-fh3-GQtPVjZjI14UbsvlbmHuIIl65qf91t2FcLbdY130_assertion description "[Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79710.RAk-fh3-GQtPVjZjI14UbsvlbmHuIIl65qf91t2FcLbdY130_provenance.
- NP79711.RAnIH6Xok1YF6N41vnKoFnaGqcxZplEaBQTQJvbun1tOk130_assertion description "[Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79711.RAnIH6Xok1YF6N41vnKoFnaGqcxZplEaBQTQJvbun1tOk130_provenance.
- NP79715.RAtnEGRS29ORxSmWlWUNETt_2VMeltueT-4NaVZwTJ8Kk130_assertion description "[Chromosome aberrations in workers exposed to organic solvents: Influence of polymorphisms in xenobiotic-metabolism and DNA repair genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79715.RAtnEGRS29ORxSmWlWUNETt_2VMeltueT-4NaVZwTJ8Kk130_provenance.
- NP79718.RAirmlyv-Qpob2IQVenK51XqHusZMwgLlA0tN5Z5TardA130_assertion description "[Double-strand break DNA repair genotype predictive of later mortality and cancer incidence in a cohort of non-smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79718.RAirmlyv-Qpob2IQVenK51XqHusZMwgLlA0tN5Z5TardA130_provenance.
- NP79722.RAlswl7u0nDmiUQ8N4gmhbe_33X-XlSsojuk9EAMCCQGE130_assertion description "[Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79722.RAlswl7u0nDmiUQ8N4gmhbe_33X-XlSsojuk9EAMCCQGE130_provenance.
- NP79732.RAiWjsjaXooi6vaS4i1JHlzQ__KGQsg4wrz_ltS-4c2Og130_assertion description "[Polymorphisms in metabolic GSTP1 and DNA-repair XRCC1 genes with an increased risk of DNA damage in pesticide-exposed fruit growers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79732.RAiWjsjaXooi6vaS4i1JHlzQ__KGQsg4wrz_ltS-4c2Og130_provenance.
- NP79734.RAlI7_h9D77SdqbXpB0MsDYktlThN9qGj1zd2AlUvcBKI130_assertion description "[our data suggest that the genotypes of CYP2E1, XRCC1 194, and XPD 751 were associated with the level of DNA damage and may contribute to individual sensitivity to DNA damage induced by VCM in the workplace.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79734.RAlI7_h9D77SdqbXpB0MsDYktlThN9qGj1zd2AlUvcBKI130_provenance.
- NP79737.RAk3enPVJB9PjkqH1EjRMJ3L9ezS6UMQNkw9GmkSXT2z4130_assertion description "[Polymorphism of XRCC1 codon arg 399 Gln is associated with higher susceptibility to endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79737.RAk3enPVJB9PjkqH1EjRMJ3L9ezS6UMQNkw9GmkSXT2z4130_provenance.
- NP79741.RAk-oKM1BsTq8qqrgFG5nmvOwy9ID27A08UJ2ouSOYrX0130_assertion description "[Single nucleotide polymorphisms in base-excision repair genes hOGG1, APE1 and XRCC1 do not alter risk of Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79741.RAk-oKM1BsTq8qqrgFG5nmvOwy9ID27A08UJ2ouSOYrX0130_provenance.
- NP79752.RAlu8SRGZQ2Ijt-fNRVf9aMpcrFv5b9q8Tz9bx9m2LCb0130_assertion description "[BRCA1 and XRCC1 polymorphisms associated with survival in advanced gastric cancer treated with taxane and cisplatin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79752.RAlu8SRGZQ2Ijt-fNRVf9aMpcrFv5b9q8Tz9bx9m2LCb0130_provenance.
- NP79764.RApSJJaIz1PuM3bTz-7sh_LpVORhMUXzsiDvxcglm8paM130_assertion description "[Candidate gene association studies and risk of childhood acute lymphoblastic leukemia: a systematic review and meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79764.RApSJJaIz1PuM3bTz-7sh_LpVORhMUXzsiDvxcglm8paM130_provenance.
- NP79765.RAisHSE9Q4oFgJ_VBVk44FGETYEhyv4PQ0WIFAw4jGRvE130_assertion description "[Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79765.RAisHSE9Q4oFgJ_VBVk44FGETYEhyv4PQ0WIFAw4jGRvE130_provenance.
- NP79767.RAkwMjDuYVWR2Y9zsmC4L_7UTy5UZN9t2zIe39AhJLH6c130_assertion description "[The XRCC1 194Trp variant allele may be associated with increased risk of DTC, while the XRCC1 399Gln variant allele may be associated with decreased risk of DTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79767.RAkwMjDuYVWR2Y9zsmC4L_7UTy5UZN9t2zIe39AhJLH6c130_provenance.
- NP79772.RAoZja_zpLdE_x_XlptJtUdRK5YraeCidOtTjtWGBz9mk130_assertion description "[Chromosome aberrations in workers exposed to organic solvents: Influence of polymorphisms in xenobiotic-metabolism and DNA repair genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79772.RAoZja_zpLdE_x_XlptJtUdRK5YraeCidOtTjtWGBz9mk130_provenance.
- NP79786.RAkeQXOq-iGE8lpYM2OUaZBV20D3ScJcrnr5ORCZbO_7k130_assertion description "[The frequency of XRCC1 haplotype B (194Arg-280Arg-399Gln) was significantly higher in DLBCL patients compared to controls (OR, 1.38; 95% CI, 1.05-1.80; P = 0.019).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79786.RAkeQXOq-iGE8lpYM2OUaZBV20D3ScJcrnr5ORCZbO_7k130_provenance.
- NP79788.RAsYX8QE9KvswjSzBF0YbOdc7_ToPSZ0wtDmjrK4zCTYQ130_assertion description "[there was no significant association between 33512C (9,091 patients and 11,553 controls) and cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79788.RAsYX8QE9KvswjSzBF0YbOdc7_ToPSZ0wtDmjrK4zCTYQ130_provenance.
- NP79791.RAsGJijPB2swAGS9dNCzNo3uTeL99PSjHjibHZz_BC5-o130_assertion description "[Micronuclei and chromosomal aberrations, important markers of ageing: possible association with XPC and XPD polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79791.RAsGJijPB2swAGS9dNCzNo3uTeL99PSjHjibHZz_BC5-o130_provenance.
- NP79795.RAowPMDriethzoYMhVCA9dyumheekS2ZqkapKihKkbNfE130_assertion description "[common genetic variations in NER genes can significantly modify laryngeal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79795.RAowPMDriethzoYMhVCA9dyumheekS2ZqkapKihKkbNfE130_provenance.
- NP79806.RAnk5ZmRgybthlwW-j7092xqva5mu4FF4x7lAk2lTIv6E130_assertion description "[Population pharmacokinetic and pharmacogenetic analysis of 6-mercaptopurine in paediatric patients with acute lymphoblastic leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79806.RAnk5ZmRgybthlwW-j7092xqva5mu4FF4x7lAk2lTIv6E130_provenance.
- NP79821.RAqe6-BV2wYEZMfxcPuvV5QmJqRCK18_JRCJb4csnpG_U130_assertion description "[WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79821.RAqe6-BV2wYEZMfxcPuvV5QmJqRCK18_JRCJb4csnpG_U130_provenance.
- NP79823.RAguN2SEVi36-LlUW6OZxp971PzcXztpY1sNrwOyhrSkM130_assertion description "[Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79823.RAguN2SEVi36-LlUW6OZxp971PzcXztpY1sNrwOyhrSkM130_provenance.
- NP79826.RAnDSt_1fIyuE-Jak5UIZBJ_FdhcZzDm1ewW8eLgvhfJM130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79826.RAnDSt_1fIyuE-Jak5UIZBJ_FdhcZzDm1ewW8eLgvhfJM130_provenance.
- NP79837.RAgDYjP6js6QUkHdj70OJI7nHffrRPu-xhUDE93FzQF2M130_assertion description "[Wnt signaling genes are associated with impaired lung function in two childhood asthma cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79837.RAgDYjP6js6QUkHdj70OJI7nHffrRPu-xhUDE93FzQF2M130_provenance.
- NP79850.RAkq6Gl21an7fv4BzPJVU5OY-yXdk-dGfKr3VS1vvCiM8130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79850.RAkq6Gl21an7fv4BzPJVU5OY-yXdk-dGfKr3VS1vvCiM8130_provenance.
- NP79856.RAizbaDpH-IOayuSKYIFrt1PA4-l-RCF9k2AtanWtEQWY130_assertion description "[Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79856.RAizbaDpH-IOayuSKYIFrt1PA4-l-RCF9k2AtanWtEQWY130_provenance.
- NP79868.RAnBtQydSBWJBx-ugMA1AfYvkGSWr8zZXeiICG-iZrSiQ130_assertion description "[We excluded mutation in 21 biological candidate genes as a common cause of primary lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79868.RAnBtQydSBWJBx-ugMA1AfYvkGSWr8zZXeiICG-iZrSiQ130_provenance.
- NP79875.RAlI7HpxEoN9XJzkuKvftYzCxgKOo0w6bwdOrakoxVqF4130_assertion description "[As these two SNPs were previously observed to be related to production of the VEGF protein, we suppose that these VEGF polymorphisms -- interacting with other genetic and environmental factors - could play a role in the development of HELLP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79875.RAlI7HpxEoN9XJzkuKvftYzCxgKOo0w6bwdOrakoxVqF4130_provenance.
- NP79878.RAtVIV_brR3ToiXU_XYfKkLSnDwKLk-4jVf22jOY8Pe5Q130_assertion description "[There were no significant differences between pterygium and control groups in age, sex, and distribution of genotype and allelic frequency of VEGF-460 polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79878.RAtVIV_brR3ToiXU_XYfKkLSnDwKLk-4jVf22jOY8Pe5Q130_provenance.
- NP79882.RAgq2sOpQr6Y62bi9cVlnPZfbxUoSHkfd15lJqD2cAnn0130_assertion description "[Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79882.RAgq2sOpQr6Y62bi9cVlnPZfbxUoSHkfd15lJqD2cAnn0130_provenance.
- NP79884.RAvCpwJ9ZeZOnWLoaBoc8QjbO6aPMClIHVfxD4gyMA5m8130_assertion description "[Genetic profiling of genes from the oxidative stress pathway among North and South Indians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79884.RAvCpwJ9ZeZOnWLoaBoc8QjbO6aPMClIHVfxD4gyMA5m8130_provenance.
- NP79887.RAucsom1peiXS5vDOQ4DDnEwAqcsGAywpAnPwMJnPBsoY130_assertion description "[cIMT is increased in patients with hyperhomocysteinemia, inflammation and extended CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79887.RAucsom1peiXS5vDOQ4DDnEwAqcsGAywpAnPwMJnPBsoY130_provenance.
- NP79889.RAu4Paf5UGBpL_lS3KCeNbjsLREDQdZiRtQ3DGM65Tx-g130_assertion description "[We have identified a novel locus in the MHC associated with CAD. MHC genes regulate inflammation and T-cell responses that contribute importantly to the initiation and propagation of atherosclerosis. Further laboratory studies will be required to understand the biological basis of this association and identify the causative allele(s).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79889.RAu4Paf5UGBpL_lS3KCeNbjsLREDQdZiRtQ3DGM65Tx-g130_provenance.
- NP79894.RAsRWPdcoW1Wx8bIbXAZ_HWSBdT8lcoyYP05OsaTW-YTw130_assertion description "[Polymorphism of vascular endothelial growth factor (VEGF) influences the VEGF responsiveness and is implicated in various types of diseases with a putative angiogenic basis, but its role in nasopharyngeal carcinoma (NPC) is not fully understood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79894.RAsRWPdcoW1Wx8bIbXAZ_HWSBdT8lcoyYP05OsaTW-YTw130_provenance.
- NP79895.RAoBPXy-HJuI2BxR4hriRnuYgXGKxGjJh5pZ62m8nbw1c130_assertion description "[Factors regulating circulating vascular endothelial growth factor (VEGF): association with bone mineral density (BMD) in post-menopausal osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79895.RAoBPXy-HJuI2BxR4hriRnuYgXGKxGjJh5pZ62m8nbw1c130_provenance.
- NP79900.RAgKV4fNgoHZ1Rs_-YFaEteQTMFAM7sGW6m3qo2sKPowA130_assertion description "[The aim of the present study was to analyze the influence of VEGF-A gene polymorphisms on tumoral VEGF-A expression and to test their prognostic value in head and neck cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79900.RAgKV4fNgoHZ1Rs_-YFaEteQTMFAM7sGW6m3qo2sKPowA130_provenance.
- NP79906.RAm9AchIv-tfpojH1Ofjo6D_9C7K92Q9Ve-pKqq1JTnjM130_assertion description "[BC is associated with markers of endothelial function and inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79906.RAm9AchIv-tfpojH1Ofjo6D_9C7K92Q9Ve-pKqq1JTnjM130_provenance.
- NP79907.RAlk45ucFV5XlKiyizYaz2qRIIuXvLuibPwiWHEgI66ko130_assertion description "[Vascular endothelial growth factor polymorphisms in mantle cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79907.RAlk45ucFV5XlKiyizYaz2qRIIuXvLuibPwiWHEgI66ko130_provenance.
- NP79916.RAjPwUZggAKj2gRwGpS6tchEJmHQJmJRmC2wD0s0rgQ70130_assertion description "[There was no main effect of vitamin D level on overall survival in the advanced NSCLC population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79916.RAjPwUZggAKj2gRwGpS6tchEJmHQJmJRmC2wD0s0rgQ70130_provenance.
- NP79920.RAkykw-yO1bSeLOwpqkohgNifm234sb2EELsQ43I0K_Ow130_assertion description "[Genetic variation in calcium-sensing receptor and risk for colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79920.RAkykw-yO1bSeLOwpqkohgNifm234sb2EELsQ43I0K_Ow130_provenance.
- NP79921.RAiJeNi0N0s_k7EpQl2bTsr4fkzOgOPL2da6zanSicTxg130_assertion description "[These data suggest that molecular variants of the VDR gene may be related to the development of colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79921.RAiJeNi0N0s_k7EpQl2bTsr4fkzOgOPL2da6zanSicTxg130_provenance.
- NP79926.RAnhm-hUWZ9hFNQSpCqVzay3dgUIJua_lZdX2ANakzSnk130_assertion description "[Vitamin D receptor gene polymorphisms predict acquired resistance to clodronate treatment in patients with Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79926.RAnhm-hUWZ9hFNQSpCqVzay3dgUIJua_lZdX2ANakzSnk130_provenance.
- NP79928.RApYljteo50QPRSGHD9JXzSFKT9WHADTCbGj5aKu1MbCc130_assertion description "[The BsmI site polymorphism of vitamin D receptor gene may be associated with abnormal growth pattern and low bone mass in girls with AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79928.RApYljteo50QPRSGHD9JXzSFKT9WHADTCbGj5aKu1MbCc130_provenance.
- NP79930.RAsiHVs0hO_K9ruDjn8G2qFMockeiNHg9tJNH2TR8OqlY130_assertion description "[Our data support the association between the TT genotype and susceptibility to LL in this Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79930.RAsiHVs0hO_K9ruDjn8G2qFMockeiNHg9tJNH2TR8OqlY130_provenance.
- NP79946.RAmVhUtwvTOLepGm0C9hdRkqm82aSewXspXJrgFE-bzf0130_assertion description "[Our study has identified a rare VDR haplotype that is protective against DN in patients with type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79946.RAmVhUtwvTOLepGm0C9hdRkqm82aSewXspXJrgFE-bzf0130_provenance.
- NP79948.RAvQCNFSyDMKtKczRdxXjQTL85wFCKoqyIsWCMRAG5tqg130_assertion description "[We excluded mutation in 21 biological candidate genes as a common cause of primary lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79948.RAvQCNFSyDMKtKczRdxXjQTL85wFCKoqyIsWCMRAG5tqg130_provenance.
- NP79949.RAmjFVZ2-kFEjcfs-YkTvmmeA04LPNR4nnSugCj9MbkiY130_assertion description "[Intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) may be important contributors to the development and progression of atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79949.RAmjFVZ2-kFEjcfs-YkTvmmeA04LPNR4nnSugCj9MbkiY130_provenance.
- NP79965.RAgH0E2Fr5RoiLFxatN4ZRm9AoiwJO_5u5ZUXw2pVuUsw130_assertion description "[Association between polymorphisms in the vesicle-associated membrane protein-associated protein A (VAPA) gene on chromosome 18p and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79965.RAgH0E2Fr5RoiLFxatN4ZRm9AoiwJO_5u5ZUXw2pVuUsw130_provenance.
- NP79976.RAhIRtErgsmgAm41AimPuuNDTtbYa_Wr4gtXWh4j-3IMw130_assertion description "[Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79976.RAhIRtErgsmgAm41AimPuuNDTtbYa_Wr4gtXWh4j-3IMw130_provenance.
- NP79995.RAsUg69y5lOqtxkxjpI7h_wYWy9NkW259rgux5xU55v5g130_assertion description "[our data suggest a genetic and functional association of PBX1 with BMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79995.RAsUg69y5lOqtxkxjpI7h_wYWy9NkW259rgux5xU55v5g130_provenance.
- NP79998.RAukyCxUdr8hjx6MSG9GC99lu9--Twyd1-UeUZQIFlGM8130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79998.RAukyCxUdr8hjx6MSG9GC99lu9--Twyd1-UeUZQIFlGM8130_provenance.
- NP80002.RAlqdO_eMqoadvhG59k8cA4Nt1TgzEkuPPf9eYe3Sr1yE130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80002.RAlqdO_eMqoadvhG59k8cA4Nt1TgzEkuPPf9eYe3Sr1yE130_provenance.
- NP80003.RAhS07aDr6ULLN4KHUFGoQL0-jct9MRj-kfwymNpSiLH8130_assertion description "[Analyzing common gene deletions in three HSCT cohorts (1,345 HLA-identical sibling donor-recipient pairs), we found that risk of acute GVHD was greater (odds ratio (OR) = 2.5; 95% confidence interval (CI) 1.4-4.6) when donor and recipient were mismatched for homozygous deletion of UGT2B17, a gene expressed in GVHD-affected tissues and giving rise to multiple histocompatibility antigens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80003.RAhS07aDr6ULLN4KHUFGoQL0-jct9MRj-kfwymNpSiLH8130_provenance.
- NP80005.RAlZyt15ilHtycsz-CvkxJr103NqGoU1CfnkS06M1g7rY130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80005.RAlZyt15ilHtycsz-CvkxJr103NqGoU1CfnkS06M1g7rY130_provenance.
- NP80009.RAniA8vdpkGSMBqm78WpObTAuDzETPIZOH88bF_kvyLCg130_assertion description "[Predictive role of the UGT1A1, UGT1A7, and UGT1A9 genetic variants and their haplotypes on the outcome of metastatic colorectal cancer patients treated with fluorouracil, leucovorin, and irinotecan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80009.RAniA8vdpkGSMBqm78WpObTAuDzETPIZOH88bF_kvyLCg130_provenance.
- NP80014.RAjh9qPa5j08gZhF63wyw4fKnRP7X6AZ2ReBZ4cSAKqQQ130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80014.RAjh9qPa5j08gZhF63wyw4fKnRP7X6AZ2ReBZ4cSAKqQQ130_provenance.
- NP80016.RAlwiKW5AsL9Ngsh69zptIP_jBXd8tXzWGHAg2oG6EdoU130_assertion description "[Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80016.RAlwiKW5AsL9Ngsh69zptIP_jBXd8tXzWGHAg2oG6EdoU130_provenance.
- NP80017.RAspbsKmGLIw2ZAV4qiCyw5tMtoqNlNaumISgRIlHrr98130_assertion description "[Uridine diphosphoglucuronosyltransferase 1A7 gene polymorphism and susceptibility to chromosomal damage among polycyclic aromatic hydrocarbons exposed workers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80017.RAspbsKmGLIw2ZAV4qiCyw5tMtoqNlNaumISgRIlHrr98130_provenance.
- NP80018.RAlJEFB-LG47zqkY7XeXMIHT8LrDdxm_mljuks8E7f-aY130_assertion description "[Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80018.RAlJEFB-LG47zqkY7XeXMIHT8LrDdxm_mljuks8E7f-aY130_provenance.
- NP80021.RAq5WyB103U5N0hHtDTwEBNxSivdIvMcYJdDHKETptNtE130_assertion description "[Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80021.RAq5WyB103U5N0hHtDTwEBNxSivdIvMcYJdDHKETptNtE130_provenance.
- NP80025.RArO_TYW-0DMdCvRjLZkJsQh6BRFmidboAt0cioHMCSc0130_assertion description "[Genetic polymorphisms in UDP-glucuronosyltransferase 1A6 are not associated with NSAIDs-related peptic ulcer haemorrhage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80025.RArO_TYW-0DMdCvRjLZkJsQh6BRFmidboAt0cioHMCSc0130_provenance.
- NP80030.RAmpbnkpkQ3PXMq7kcTxw6yxH-i7g5DaPpNQt1p8aINsA130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80030.RAmpbnkpkQ3PXMq7kcTxw6yxH-i7g5DaPpNQt1p8aINsA130_provenance.
- NP80031.RAkmWZbOJB5CTIkKkjjm4fSwWweo1fnOLxT4L2Nlf0zng130_assertion description "[PTEN identified as important risk factor of chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80031.RAkmWZbOJB5CTIkKkjjm4fSwWweo1fnOLxT4L2Nlf0zng130_provenance.
- NP80032.RAhV0Hpf3evm8E9y-Ey27ud_2mkmhUi8sx4lZHXv0dygc130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80032.RAhV0Hpf3evm8E9y-Ey27ud_2mkmhUi8sx4lZHXv0dygc130_provenance.
- NP80041.RAnPUdAfNLIdjnCfo0eAVk-gOzV_OZxXiLqK9uNtp9ek8130_assertion description "[Effects of UGT1A1*28 polymorphism on raloxifene pharmacokinetics and pharmacodynamics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80041.RAnPUdAfNLIdjnCfo0eAVk-gOzV_OZxXiLqK9uNtp9ek8130_provenance.
- NP80043.RAs3rRYSlHtUE7GAp1LjIJojKVEyOrt_PH7G9lNBYh-SU130_assertion description "[Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80043.RAs3rRYSlHtUE7GAp1LjIJojKVEyOrt_PH7G9lNBYh-SU130_provenance.
- NP80044.RAukWBZvOcKIGRXyj0NBOJL-ksmhQ7TEANENSpd-TL7s8130_assertion description "[Genetic polymorphisms of drug-metabolizing enzymes and anti-TB drug-induced hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80044.RAukWBZvOcKIGRXyj0NBOJL-ksmhQ7TEANENSpd-TL7s8130_provenance.
- NP80049.RAr6qIh0EY2AZqt7Iq2zhAm7GF4mfhc9clWRS07fZZN04130_assertion description "[Genetic factors associated with rheumatoid arthritis and systemic vasculitis: Evaluation of a panel of polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80049.RAr6qIh0EY2AZqt7Iq2zhAm7GF4mfhc9clWRS07fZZN04130_provenance.