Nanopublications LDF server

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

• NP53655.RAtENRb7Ix4W4c0JQMgXHemVcXGvu-1iVxixLWota-2GM130_assertion description "[Polymerase chain reaction-restriction fragment length polymorphism-based genotyping assays were used to determine the frequency of polymorphisms in EPHX1 (exons 3 and 4), NQO1 (exon 6), GSTM1 (deletion), GSTP1 (exon 5), and GSTT1 (deletion) in a case-control study comprised of 238 patients with breast cancer and 313 healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53655.RAtENRb7Ix4W4c0JQMgXHemVcXGvu-1iVxixLWota-2GM130_provenance.
• NP53657.RAk2XGSJ45NbmpXPEz5kZ6X91pHudrnAOCHaBLN994Q7I130_assertion description "[Overall, there is no conclusive evidence that genetic variants in genes involved in the estrogen metabolic pathway are associated with mammographic density in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53657.RAk2XGSJ45NbmpXPEz5kZ6X91pHudrnAOCHaBLN994Q7I130_provenance.
• NP53659.RAkUM6RjTfYWVKzA0nt6uBXd9pPtoZVBy8x_mZbpCMX0Q130_assertion description "[Variants encoding lower activity of NOS3 may affect outcomes in breast cancer patients, with the direction of risk differing depending on chemotherapy status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53659.RAkUM6RjTfYWVKzA0nt6uBXd9pPtoZVBy8x_mZbpCMX0Q130_provenance.
• NP53670.RAu9DUSktwuhSjCaKam3IcQkbgbNFaZptuyXPuiQAirw8130_assertion description "[Tobacco and estrogen metabolic polymorphisms and risk of non-small cell lung cancer in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53670.RAu9DUSktwuhSjCaKam3IcQkbgbNFaZptuyXPuiQAirw8130_provenance.
• NP53674.RAsqsy497fzubd_7Di4UcDnoA3-iq7uItdaa5BOP7NVeI130_assertion description "[Our data suggested that the deletion of 29-bp nucleotides in the promoter region of the NQO2 gene associates with the development of PD]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53674.RAsqsy497fzubd_7Di4UcDnoA3-iq7uItdaa5BOP7NVeI130_provenance.
• NP53679.RAjKlOJZVA4zEITw5IlsI1IYJSXG-Qy2CIuEJlCnMlBrc130_assertion description "[A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53679.RAjKlOJZVA4zEITw5IlsI1IYJSXG-Qy2CIuEJlCnMlBrc130_provenance.
• NP53680.RArhI3DLOOvSdcnABnyU8Bqc4raLSydFc0waiK4kZXc8k130_assertion description "[The CYP1A1*2B allele may predispose to the development of these sub-groups of AML by augmented phase 1 metabolism to highly reactive intermediates of CYP1A1 substrates including polycyclic aromatic hydrocarbons or by generation of oxidative stress as a metabolic by-product.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53680.RArhI3DLOOvSdcnABnyU8Bqc4raLSydFc0waiK4kZXc8k130_provenance.
• NP53682.RAvqtU0kAWtCptDhpULYm159mnD2Flv-lqwJbVretIIjY130_assertion description "[We investigated the role of glutathione S-transferase (GST) enzymes (M1, T1), methylenetetrahydrofolate (MTHFR) 677 and 1298, and the NAD(P)H:quinone oxidoreductase (NQO1) polymorphisms in a population-based bladder cancer case-control study in Argentina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53682.RAvqtU0kAWtCptDhpULYm159mnD2Flv-lqwJbVretIIjY130_provenance.
• NP53683.RAiRHKP_vMOqo75eqZj7up6yIexsgNHsmOBO1GcOuiKHs130_assertion description "[These findings suggest that individual susceptibility of bladder cancer may be modulated by MPO and MnSOD polymorphisms, and that the combination of genetic factors involved in oxidative stress response with environmental carcinogens may play an important role in bladder carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53683.RAiRHKP_vMOqo75eqZj7up6yIexsgNHsmOBO1GcOuiKHs130_provenance.
• NP53684.RAjhPK0kU9e1X_YwtK5iqE7G_Yy9BcAhRLeWh3eiDrvDg130_assertion description "[These results suggest that the NQO1 genetic polymorphism modulates bladder cancer risk, especially in men and ever smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53684.RAjhPK0kU9e1X_YwtK5iqE7G_Yy9BcAhRLeWh3eiDrvDg130_provenance.
• NP53685.RAo-g2ybySSViqosXueEuiPJ4OfBwRzIkDH2wqnhRPsYU130_assertion description "[Bladder cancer risk and genetic variation in AKR1C3 and other metabolizing genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53685.RAo-g2ybySSViqosXueEuiPJ4OfBwRzIkDH2wqnhRPsYU130_provenance.
• NP53690.RAnmRxjpN3dTnRAQg5myePhoMK8hg5Qd_aFAH2Ti_-owE130_assertion description "[We investigated the prognostic significance of genetic polymorphism in glutathione-S transferase mu 1 (GSTM1), glutathione-S transferase theta 1 (GSTT1), NAD(P)H:quinone oxidoreductase (NQO1) and myeloperoxidase (MPO), the products of which are associated with drug metabolism as well as with detoxication, in 193 patients with de novo acute myeloid leukemia (AML) other than M3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53690.RAnmRxjpN3dTnRAQg5myePhoMK8hg5Qd_aFAH2Ti_-owE130_provenance.
• NP53699.RAk9Ea3ujjnpJ6rYH0pbJoc-ZB4a_IBLrqVR610TqG-ok130_assertion description "[We examined asthma prevalence and evaluated polymorphisms in genes involved in oxidative stress pathways gluthatione S-transferases M1 (GSTM1), T1 (GSTT1), and P1 (GSTP1) and NAD(P)H:quinine oxidoreductase (NQO1), inflammatory response tumor necrosis factor alpha (TNFA), immunologic response Toll-like receptor 4 (TLR4), and airway reactivity adrenergic receptor beta2 (ADRB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53699.RAk9Ea3ujjnpJ6rYH0pbJoc-ZB4a_IBLrqVR610TqG-ok130_provenance.
• NP53708.RAijOmYDMOyGV9aPdkEBJ7m5tEWNPtKu55dyaLsQiEP2I130_assertion description "[ The cDNA 609 T allele of NQO1 gene is very likely to be associated with the genetic susceptibility to nasopharyngeal carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53708.RAijOmYDMOyGV9aPdkEBJ7m5tEWNPtKu55dyaLsQiEP2I130_provenance.
• NP53714.RAtBl0fGWnG43RqIjsbh2zwWxliX2vT1F57vqhyjCbVOM130_assertion description "[ Pro7 does not seem to be associated with a diagnosis of alcoholism in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53714.RAtBl0fGWnG43RqIjsbh2zwWxliX2vT1F57vqhyjCbVOM130_provenance.
• NP53729.RAsEw1jWASGmy7RqbiVcQvdvXBZxWdRKwIj8ikbkJgtVI130_assertion description "[ Our data suggested that a C to T substitution at the 5671 locus of the NPY gene may be associated with seizure during alcohol withdrawal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53729.RAsEw1jWASGmy7RqbiVcQvdvXBZxWdRKwIj8ikbkJgtVI130_provenance.
• NP53730.RAsQdwzKO0vhBSf96t4MEZkLL6X_YfCnk6vjKA_CKx8Oc130_assertion description "[The role of DRD2 and NPY on alcohol dependence was also supported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53730.RAsQdwzKO0vhBSf96t4MEZkLL6X_YfCnk6vjKA_CKx8Oc130_provenance.
• NP53732.RAgrRdB5kESdvnqW3kfb4d0GP0I5ZhIB_5PYC3wb1ejWc130_assertion description "[Decreased cerebrospinal fluid neuropeptide Y (NPY) in patients with treatment refractory unipolar major depression: preliminary evidence for association with preproNPY gene polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53732.RAgrRdB5kESdvnqW3kfb4d0GP0I5ZhIB_5PYC3wb1ejWc130_provenance.
• NP53734.RAmS75s_z4aka430FcKBMJQMdCvbqzoXieJ15Xf2ACx5c130_assertion description "[Neuropeptide Y (NPY) has been found to play a role in the pathomechanism of both anxiety and depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53734.RAmS75s_z4aka430FcKBMJQMdCvbqzoXieJ15Xf2ACx5c130_provenance.
• NP53758.RAm5ZIgLIUEiYz8UTxHJ9mHV7QZGhNd4IlQ_o4IZf0HYo130_assertion description "[This suggests that: 1) this I/D dimorphism is not a useful marker to study the relationship between the ANF gene and hypertension in the UAE; and 2) variations of the ANF gene that may be in linkage disequilibrium with this marker do not play a major role in the determination of hypertension in this Arab population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53758.RAm5ZIgLIUEiYz8UTxHJ9mHV7QZGhNd4IlQ_o4IZf0HYo130_provenance.
• NP53766.RAuNvdI3l6-3nsW_ODDwmzIAh_Oi5xUNuu41NPnouPPd4130_assertion description "[ Although the present results should be replicated in other study populations for confirmation, the present results suggest that SLC12A1 may contribute to hypertension in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53766.RAuNvdI3l6-3nsW_ODDwmzIAh_Oi5xUNuu41NPnouPPd4130_provenance.
• NP53768.RAuD4mp7_m3ghbqxd5jitf9pQXtyuQRGWfKtQBfERyK7A130_assertion description "[Nucleophosmin (NPM) is a nucleocytoplasmic shuttling protein involved in leukemia-associated chromosomal translocations, and it regulates the alternate reading frame (ARF)-p53 tumor-suppressor pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53768.RAuD4mp7_m3ghbqxd5jitf9pQXtyuQRGWfKtQBfERyK7A130_provenance.
• NP53773.RAjePSJPufGNDKb7dRfHRudNTx0UyPKuyY9_8kNGB5ExQ130_assertion description "[In conclusion, this study demonstrates that NPM1+/FLT3-LM- mutations are an independent predictor for a favorable outcome in AML with normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53773.RAjePSJPufGNDKb7dRfHRudNTx0UyPKuyY9_8kNGB5ExQ130_provenance.
• NP53774.RAmSbkGEfvr93ipjjVSoXrpdW3J0PJRUHTKJdUw18f_hQ130_assertion description "[Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53774.RAmSbkGEfvr93ipjjVSoXrpdW3J0PJRUHTKJdUw18f_hQ130_provenance.
• NP53775.RApTVTSyXhSRPVXVddfEfySwrADQuat_JwTYnTG2X8ThE130_assertion description "[Hence, in addition to conventional karyotyping and RT-PCR of fusion genes, combined analysis of both Flt3 and NPM1 mutations will be increasingly relevant in the genetic diagnosis work-up of AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53775.RApTVTSyXhSRPVXVddfEfySwrADQuat_JwTYnTG2X8ThE130_provenance.
• NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion description "[ The results demonstrate that NPHS2 mutations are also present in Chinese sporadic SRNS. Our investigation supports the necessity of searching for mutations in NPHS2 in Chinese children with sporadic SRNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.
• NP53779.RAnh9AyLjMialLdlaQmbECEjQwNsONSnBZ9LxUeG-MLsw130_assertion description "[ These results suggest that uncommon variants of the NPHS2 gene may play a role in the development of nondiabetic ESRD in AAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53779.RAnh9AyLjMialLdlaQmbECEjQwNsONSnBZ9LxUeG-MLsw130_provenance.
• NP53783.RAiW0Bw19mP_85GJ1T5cF3uld1zTqc-90wGTqfXIRfuOU130_assertion description "[Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53783.RAiW0Bw19mP_85GJ1T5cF3uld1zTqc-90wGTqfXIRfuOU130_provenance.
• NP53785.RAnYHuOTGhVo2qU1G5pYPE39UCqvlHhRtlHktHKaJ2V78130_assertion description "[Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53785.RAnYHuOTGhVo2qU1G5pYPE39UCqvlHhRtlHktHKaJ2V78130_provenance.
• NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_assertion description "[Two siblings affected with a mild form of JS were found to have a homozygous deletion of the NPHP1 gene identical, by mapping, to that in subjects with NPHP alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53787.RApnrnA30iH6B6eQD0TE86Q585nW5h-_2-QhjaJMy5dFU130_provenance.
• NP53796.RAoMaQKBrHvSVEJVOjSTRgfthHR58vbvNZ3LdNR3OGZz8130_assertion description "[Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53796.RAoMaQKBrHvSVEJVOjSTRgfthHR58vbvNZ3LdNR3OGZz8130_provenance.
• NP53797.RAhjBMqe7VWL8on06E4zYn2Y0LvzZqPDUNxmUplHbbcnw130_assertion description "[Association study between the TNXB locus and schizophrenia in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53797.RAhjBMqe7VWL8on06E4zYn2Y0LvzZqPDUNxmUplHbbcnw130_provenance.
• NP53799.RAnyrE5yjCFsCutuUufD2vDn8xHgsLn0T4aqRyWOgCaJo130_assertion description "[ No association between two NOTCH4 polymorphisms alone and Alzheimer's disease was observed in the three populations, but there was evidence of an increased risk associated with the 5'-UTR CC genotype in epsilon 4 bearers in the United Kingdom. As no functionality for this polymorphism could be determined, it is likely that the interaction is spurious or results from a linkage disequilibrium of this 5'-UTR polymorphism with another marker elsewhere in the 6p21.3 locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53799.RAnyrE5yjCFsCutuUufD2vDn8xHgsLn0T4aqRyWOgCaJo130_provenance.
• NP53801.RApVYIdGQRqiNezVyT7UNUmIXo2bu_yZXp_kY9Ne6u1EE130_assertion description "[ Notch3 mutations are rare in patients with typical strokes due to cerebral small-vessel disease. In the absence of classic features suggestive of CADASIL, screening for Notch3 mutations has a low yield.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53801.RApVYIdGQRqiNezVyT7UNUmIXo2bu_yZXp_kY9Ne6u1EE130_provenance.
• NP53810.RAi2WkCqF73xw2b70JX9p_RaA_GsPDJ9jUPQgf4t4fA4I130_assertion description "[Previous epidemiological studies have demonstrated a protective association between the NOS2G-954C (NOS2(Lambarn)) polymorphism in inducible nitric oxide synthase and severe malaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53810.RAi2WkCqF73xw2b70JX9p_RaA_GsPDJ9jUPQgf4t4fA4I130_provenance.
• NP53814.RAikqT9I1wx68ajHo-GNIknoK_rFNwcbAyD__aBCPs0T8130_assertion description "[, we found that the NOS2A (CCTTT)(14) allele was detected more frequently in the control group than in the RRMS patients, thus confirming the scientific interest on this marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53814.RAikqT9I1wx68ajHo-GNIknoK_rFNwcbAyD__aBCPs0T8130_provenance.
• NP53823.RAjMAXjkn9luMsi9vcmO-FVsXwzEOG-5JbtitagZ4lj4Y130_assertion description "[Neither the G-954C nor the C-1173T polymorphisms were identified in this population, indicating the variability and complexity of selection for NOS2 promoter polymorphisms in different malaria-endemic populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53823.RAjMAXjkn9luMsi9vcmO-FVsXwzEOG-5JbtitagZ4lj4Y130_provenance.
• NP53826.RAu7BOB-J2oLgdRBFjw0ew1YaYmhVsGRatAnxpjtWNix8130_assertion description "[ iNOS Ser(608)Leu allele may be a potential determinant of susceptibility to cigarette -alcohol induced gastric cancer, but larger studies are needed to confirm the observations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53826.RAu7BOB-J2oLgdRBFjw0ew1YaYmhVsGRatAnxpjtWNix8130_provenance.
• NP53829.RApk9MwVdSvhrSD76O-3jD3OGmfu4RoQObaqJn_LXm53U130_assertion description "[No significant differences in allele or genotype frequencies for the (CCTTT)n repeat polymorphism in the NOS2A gene between patients with GCA and controls were observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53829.RApk9MwVdSvhrSD76O-3jD3OGmfu4RoQObaqJn_LXm53U130_provenance.
• NP53835.RAhDWieeQPGTRPeawd5-X2ALPmK3WOS7mm81M1o2x_pkA130_assertion description "[In conclusion, these results, therefore, suggest that NOS2 promoter polymorphisms have a limited effect on the onset or progression of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53835.RAhDWieeQPGTRPeawd5-X2ALPmK3WOS7mm81M1o2x_pkA130_provenance.
• NP53836.RAp-cjABvmFznBc9ozCYUpWOWrFFd05BgfEoP_ZcKzDPM130_assertion description "[Screening of 214 single nucleotide polymorphisms in 44 candidate cancer susceptibility genes: a case-control study on gastric and colorectal cancers in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53836.RAp-cjABvmFznBc9ozCYUpWOWrFFd05BgfEoP_ZcKzDPM130_provenance.
• NP53841.RAue93eYjzGiTh2tJ410fL0905Jkh7sT0bGoUaa9H_Zbw130_assertion description "[Thus the '' allele of the NOS2A promoter variant may confer higher iNOS expression, and could contribute to complications of type 2 diabetes, especially in the approximately 5% of patients homozygous for this variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53841.RAue93eYjzGiTh2tJ410fL0905Jkh7sT0bGoUaa9H_Zbw130_provenance.
• NP53843.RAlbcJ0Cve1OySqZ0mXW1TECvIrGV9LSo7lYXm6nKPNZ0130_assertion description "[Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53843.RAlbcJ0Cve1OySqZ0mXW1TECvIrGV9LSo7lYXm6nKPNZ0130_provenance.
• NP53844.RAv6IvOqQ_zOXLs9C74tJmw5C9u6IilMiqun1Zz7FGulM130_assertion description "[Support Vector Machine based feature selection method in this research found novel association between combinations of SNPs and T2D in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53844.RAv6IvOqQ_zOXLs9C74tJmw5C9u6IilMiqun1Zz7FGulM130_provenance.
• NP53845.RAn4e07c6LMyq6uOH7mXS5vXYA4KOmY37BAStf_DRh57M130_assertion description "[The independent risk conferred by genetic variants encoding pathways such as inflammation and lipid metabolism, not adequately reflected by conventional biomarkers, may identify high-risk individuals for intensified control of modifiable risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53845.RAn4e07c6LMyq6uOH7mXS5vXYA4KOmY37BAStf_DRh57M130_provenance.
• NP53848.RAvJ7EjI-gDc5DLLopRc4Eh2HmnpqRgF0ThMekEH2qIMg130_assertion description "[ Although the present results should be replicated in other study populations for confirmation, the present results suggest that SLC12A1 may contribute to hypertension in Japanese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53848.RAvJ7EjI-gDc5DLLopRc4Eh2HmnpqRgF0ThMekEH2qIMg130_provenance.
• NP53849.RAo2l08GhcB_4rTxG_JL0mWAcKYfKXpD--2xplugAegFo130_assertion description "[Association analysis of TG repeat polymorphism of the neuronal nitric oxide synthase gene with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53849.RAo2l08GhcB_4rTxG_JL0mWAcKYfKXpD--2xplugAegFo130_provenance.
• NP53850.RAnGuN-XNkJ8p1KtL_c7_aa7ilN-vciOVzFuDtS5ctxEM130_assertion description "[We assessed the frequency of both the G-954C and CCTTT microsatellite repeat NOS2 promoter polymorphisms in a cohort of patients with SLE and age, sex, and race matched controls in North Carolina and South Carolina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53850.RAnGuN-XNkJ8p1KtL_c7_aa7ilN-vciOVzFuDtS5ctxEM130_provenance.
• NP53854.RArZuXSPFJVNsIVoXMN1Rr6ph1UqzQGInU1xZYicaEBWQ130_assertion description "[An initial cohort of 808 CF patients homozygous for the common CF mutation, DeltaF508, showed significant association for polymorphisms in the endothelin receptor A gene, EDNRA (P = 0.04), but not in the related endothelin genes (EDN1, EDN2, EDN3, or EDNRB) or NOS1, NOS2A, or NOS3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53854.RArZuXSPFJVNsIVoXMN1Rr6ph1UqzQGInU1xZYicaEBWQ130_provenance.
• NP53856.RAkVhbKteBm2QrUBPvhRqNxGvBecNF1gmIF5pOFKWpGqQ130_assertion description "[Our results strongly support a previous hypothesis that NOS1 contributes to the genetic risk of schizophrenia and suggest that further research on more NOS1 variants and its regular elements are warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53856.RAkVhbKteBm2QrUBPvhRqNxGvBecNF1gmIF5pOFKWpGqQ130_provenance.
• NP53858.RAlK4kGNklZ9auG7oINQ-LKlVPn9OVbzniHACbC-JLGAU130_assertion description "[Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53858.RAlK4kGNklZ9auG7oINQ-LKlVPn9OVbzniHACbC-JLGAU130_provenance.
• NP53859.RApX2KKZEkjDCQS1LqGZXCZqNtkLquKgMifbeCUZKToec130_assertion description "[A putative cis-acting polymorphism in the NOS1 gene is associated with schizophrenia and NOS1 immunoreactivity in the postmortem brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53859.RApX2KKZEkjDCQS1LqGZXCZqNtkLquKgMifbeCUZKToec130_provenance.
• NP53860.RAovQSBvm3qRLf6TJQFqPJdgeHvbrA4gnjCAxIT4459iQ130_assertion description "[Our data suggest complex epistatic effects implicating an NRG1 molecular pathway in cognitive brain function and the pathogenesis of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53860.RAovQSBvm3qRLf6TJQFqPJdgeHvbrA4gnjCAxIT4459iQ130_provenance.
• NP53864.RAs3RKQcsz7PFDVnWTH9RX5d0VABEl0oHDAHO4cjbTgPk130_assertion description "[However, when we included genotype at a prominent asthma candidate gene (i.e., NOS1) in the case definition, and determined the number of AAT repeats in intron 20, we identified a remarkably homogeneous cohort of patients with respect to FENO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53864.RAs3RKQcsz7PFDVnWTH9RX5d0VABEl0oHDAHO4cjbTgPk130_provenance.
• NP53875.RAkgJ7_7T3nAas6Mcm-15YGFuXNpuVT_65IVFWkmdKOOI130_assertion description "[These results indicate that mutations in NLGN3 and NLGN4 genes are responsible for at most a small fraction of autism cases and additional screenings in other autistic populations are needed to better determine the frequency with which mutations in NLGN3 and NLGN4 occur in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53875.RAkgJ7_7T3nAas6Mcm-15YGFuXNpuVT_65IVFWkmdKOOI130_provenance.
• NP53876.RAr__h7J9sOWvZ2OoKz_XqpeNKGPLogt2OWliU9QMBig8130_assertion description "[Frameshift and missense mutations in the X-linked neuroligin 4 (NLGN4, MIM# 300427) and neuroligin 3 (NLGN3, MIM# 300336) genes have been identified in patients with autism, Asperger syndrome and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53876.RAr__h7J9sOWvZ2OoKz_XqpeNKGPLogt2OWliU9QMBig8130_provenance.
• NP53877.RAms3LJH2kKbWVfSvMMCBSZzluHZptKbKq0QMhe-wM2ys130_assertion description "[A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53877.RAms3LJH2kKbWVfSvMMCBSZzluHZptKbKq0QMhe-wM2ys130_provenance.
• NP53884.RAkJ3RwGjBKedKHgJkMt1zDU7_ITvc5vtVu0zoBlpMz7Y130_assertion description "[Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53884.RAkJ3RwGjBKedKHgJkMt1zDU7_ITvc5vtVu0zoBlpMz7Y130_provenance.
• NP53893.RAtRXiG13z2FsJ_KDYwIvLZE1xEsC503Z6Z1L_Qsqf8fI130_assertion description "[ Our results suggest that LTA is one of the genes that contributes to susceptibility to atopic asthma, and that the association of the TNF/LTA haplotypes to asthma may be defined by the polymorphism in the LTA promoter region in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53893.RAtRXiG13z2FsJ_KDYwIvLZE1xEsC503Z6Z1L_Qsqf8fI130_provenance.
• NP53894.RAiEd91uiGkiLYT_xuGRk4NiRQGFAGYR-sXJKjb7Nw1O4130_assertion description "[To date, familial HL cases have not been evaluated for germline NFKBIA mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53894.RAiEd91uiGkiLYT_xuGRk4NiRQGFAGYR-sXJKjb7Nw1O4130_provenance.
• NP53903.RAtO-5AAFJitE5OiO0RLx-wYIHKm9bU5_EBEKseluCJ2Y130_assertion description "[Deletion of the polymorphism was associated with increased susceptibility to sporadic colorectal cancers in the Swedish population, but not in the Swedish patients with a family history of colorectal cancer or in Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53903.RAtO-5AAFJitE5OiO0RLx-wYIHKm9bU5_EBEKseluCJ2Y130_provenance.
• NP53904.RAueTAd4lg90kJuwHJ7BtkNJVmK8S3FcQ9fBnzXJ6UV1s130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53904.RAueTAd4lg90kJuwHJ7BtkNJVmK8S3FcQ9fBnzXJ6UV1s130_provenance.
• NP53909.RAli2UZySlq7D2A83aZFj6V6fpS1dRQW8D1O6mjHk4yf8130_assertion description "[Our findings suggest that Ki-ras and ERCC2 SNPs are possible markers for meningioma formation, whereas cyclin D1 and p16 SNPs may be markers of genes that have an inverse effect on the risk to develop meningioma in irradiated and nonirradiated populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53909.RAli2UZySlq7D2A83aZFj6V6fpS1dRQW8D1O6mjHk4yf8130_provenance.
• NP53911.RAk4IFrHwbIVzaP9toWuxWZMA7m-_EWtHSAD4D_6utujQ130_assertion description "[Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder caused by mutations in the NF2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53911.RAk4IFrHwbIVzaP9toWuxWZMA7m-_EWtHSAD4D_6utujQ130_provenance.
• NP53914.RAiu_SFWXynNwHNtGHdI5zoZ0D-EJi6I3Spca37t831uE130_assertion description "[Loss of NF1 allele in Schwann cells but not in fibroblasts derived from an NF1-associated neurofibroma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53914.RAiu_SFWXynNwHNtGHdI5zoZ0D-EJi6I3Spca37t831uE130_provenance.
• NP53915.RApT5qpu84gZN0Q3Jj7JThk9wdtP5BjznwAvFc3T5RD8Q130_assertion description "[Allelic loss of the NF1 gene in NF1-associated plexiform neurofibromas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53915.RApT5qpu84gZN0Q3Jj7JThk9wdtP5BjznwAvFc3T5RD8Q130_provenance.
• NP53916.RAqTzF6IyJ-3a_j4vxuYzm5q1wzmett72OWnmGWF04cx0130_assertion description "[beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53916.RAqTzF6IyJ-3a_j4vxuYzm5q1wzmett72OWnmGWF04cx0130_provenance.
• NP53918.RAvrBNB820jnbC-fhwCX_G19AMMnmY7ZFlR49pYFm4WOU130_assertion description "[In conclusion, the frequency of Ala45Thr polymorphism in this studied Polish population is similar to its frequency in other Caucasians. We did not find evidence that the Ala45Thr polymorphism of BETA2/NeuroD1 played a role in the risk of T2DM in the examined Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53918.RAvrBNB820jnbC-fhwCX_G19AMMnmY7ZFlR49pYFm4WOU130_provenance.
• NP53922.RAoFpNMqXSADcIT3aoySFQ8eW142E8KUXwPV-Sp9GJ5HY130_assertion description "[Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53922.RAoFpNMqXSADcIT3aoySFQ8eW142E8KUXwPV-Sp9GJ5HY130_provenance.
• NP53923.RAq74bQM2LIjJgUMPFYCV5HFyS-RI3ajYorN7pdzmBnq8130_assertion description "[Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53923.RAq74bQM2LIjJgUMPFYCV5HFyS-RI3ajYorN7pdzmBnq8130_provenance.
• NP53936.RAul3HjXZYGbXujZRcqvS7RNeG-YV6-dZjvpKknYimLxE130_assertion description "[The genetic variations of NEDD4L may be associated with essential hypertension in females in the Kazakh general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53936.RAul3HjXZYGbXujZRcqvS7RNeG-YV6-dZjvpKknYimLxE130_provenance.
• NP53938.RAhiGBNb924EogQi0ekwUj9X0Fz_tcZjAPhbW2oXPAsTM130_assertion description "[Recently, a functional polymorphism located at the last nucleotide of exon 1 (rs4149601) of the NEDD4L gene were found to be associated with hypertension both in African Americans and whites, and a `flip-flop` association with hypertension was found in two white samples for a polymorphism located at intron 13 (rs3865418).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53938.RAhiGBNb924EogQi0ekwUj9X0Fz_tcZjAPhbW2oXPAsTM130_provenance.
• NP53944.RAp5kB3mo8_acgDk8bFR3Yt1QDTiQo0ypzoNDAQQ_uIy4130_assertion description "[Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53944.RAp5kB3mo8_acgDk8bFR3Yt1QDTiQo0ypzoNDAQQ_uIy4130_provenance.
• NP53950.RAjPVVp_Y2MmzNeVuN88KHn-uP1jKi8Yr5qqj6vxLoSSY130_assertion description "[Most of the variants in the candidate breast cancer genes evaluated in this study are not strong predictors of breast density. However, our findings of differences in associations for UGT1A1 and AIB1 genotypes with breast density by menopausal status needs additional corroboration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53950.RAjPVVp_Y2MmzNeVuN88KHn-uP1jKi8Yr5qqj6vxLoSSY130_provenance.
• NP53951.RAmj34eXUFZZ45vp2oCqtW29KJ7-G5f5buNXIq8slwPnA130_assertion description "[Our data indicated no significant allelic/genotypic association between any of the five mutations and bipolar phenotype when they were considered either individually or as haplotypes. Finally, the CAG repeat observed in SMRT/N-CoR2 did not demonstrate allelic instability and consequently it is unlikely that this polymorphism could be involved in the anticipation phenomenon reported for BP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53951.RAmj34eXUFZZ45vp2oCqtW29KJ7-G5f5buNXIq8slwPnA130_provenance.
• NP53953.RAgZJvjsJULCKQ_AiQXRqoNs0feS7Dt6k1GwF1oGZXF_8130_assertion description "[The joint effect of smoking and AIB1 on breast cancer risk in BRCA1 mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53953.RAgZJvjsJULCKQ_AiQXRqoNs0feS7Dt6k1GwF1oGZXF_8130_provenance.
• NP53956.RAsXXTiqreYurmCzA-vnRFdW29EOHIx-TT0moK5MtR7qY130_assertion description "[This data illustrates the importance of coregulators, especially SRC-3, in breast cancer development and suggests that more focused studies, including functional analyses, should be conducted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53956.RAsXXTiqreYurmCzA-vnRFdW29EOHIx-TT0moK5MtR7qY130_provenance.
• NP53959.RAjtjoEQiPQ6VEjBqVWm_FHq7wVLFJtTjqdKPWsIPQxZc130_assertion description "[We systematically investigated the association of 48 SNPS in four vitamin D metabolizing genes CYP27A1, GC, CYP27B1 and CYP24A1 with serum 25-hydroxyvitamin D 25(OH)D and 1,25-dihydroxyvitamin D 1,25(OH)(2)D levels and the association of these SNPS and an additional 164 SNPS in eight downstream mediators of vitamin D signaling VDR, RXRA, RXRB, PPAR, NCOA1, NCOA2, NCOA3 and SMAD3 with prostate cancer risk in the 749 incident prostate cancer cases and 781 controls of the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53959.RAjtjoEQiPQ6VEjBqVWm_FHq7wVLFJtTjqdKPWsIPQxZc130_provenance.
• NP53961.RAnE22YdhdzsMJ9NRU88vilpa8xKmQ5P8cQo0EVL5PC3A130_assertion description "[Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53961.RAnE22YdhdzsMJ9NRU88vilpa8xKmQ5P8cQo0EVL5PC3A130_provenance.
• NP53972.RAigE96JhfrgessAVoerfnc96JgH9xoYiDwRChMHN8KCY130_assertion description "[NBS1 8360G > C polymorphism is associated with breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53972.RAigE96JhfrgessAVoerfnc96JgH9xoYiDwRChMHN8KCY130_provenance.
• NP53976.RAiDY5UAOoI1zFJbPxCKrfpiF-gCDxdVtqKVZBEHHGndU130_assertion description "[SNPs located at the gene HUS1 are good candidates for further investigation in independent association studies and functional assays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53976.RAiDY5UAOoI1zFJbPxCKrfpiF-gCDxdVtqKVZBEHHGndU130_provenance.
• NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion description "[These findings suggest that heterozygous carriers of the NBS1 founder mutation exhibit increased susceptibility to prostate cancer and that the cancers that develop in the prostates of carriers are functionally homozygous for the mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance.
• NP53987.RAo1WJZhNiKGQxdWyxZPrt1_u2S_oxHb8Xgszsjcc078M130_assertion description "[Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53987.RAo1WJZhNiKGQxdWyxZPrt1_u2S_oxHb8Xgszsjcc078M130_provenance.
• NP53990.RAiEScUFv1b5JGsrkUq-_65Q2RnsdUraJX6IW8r_-HmBs130_assertion description "[There were no statistically significant interactions between tobacco smoking and either NAT1 or NAT2 acetylator status in relation to CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53990.RAiEScUFv1b5JGsrkUq-_65Q2RnsdUraJX6IW8r_-HmBs130_provenance.
• NP53991.RAiRwESVm3dPpEXhqIp_EhRlwCGRMLOeEuoc7K7LAA_1c130_assertion description "[We investigated CYP1A1*2A, CYP1A1*2C, CYP1A2*1C, CYP1A2*1F, GSTM1 and NAT2 gene polymorphisms, involving enzymes which metabolize many carcinogens, with reference to colorectal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53991.RAiRwESVm3dPpEXhqIp_EhRlwCGRMLOeEuoc7K7LAA_1c130_provenance.
• NP53992.RAvaBGE87omFeY8p0edoP8LxZQ0yrVkYPOsvTZUMS280w130_assertion description "[Being stratified by gender factors, the colorectal cancer risk in females with homozygous W/W or Mx/W+W/W fast acetylators increased 2.47-fold and 2.13-fold compared with those with the Mx/Mx slow acetylator genotype (95 percent confidence interval, 1.27-4.82 for W/W genotype; 95 percent confidence interval, 1.17-3.89 for Mx/W+W/W genotype); however, the risk of the NAT2 genotype and colorectal cancer was not observed in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53992.RAvaBGE87omFeY8p0edoP8LxZQ0yrVkYPOsvTZUMS280w130_provenance.
• NP53993.RAvZE_6st_hB0lRYwdND4qChwVoi5F5zMk5ftRaQytLNc130_assertion description "[The association of risk for colorectal cancer and selected red and white meat mutagen indices and the use of white meat drippings, or fried white meat variables was more evident within select combinations of the CYP1A1 genotype and either the GSTM1 genotype or NAT2 than with the CYP1A1 alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53993.RAvZE_6st_hB0lRYwdND4qChwVoi5F5zMk5ftRaQytLNc130_provenance.
• NP53996.RApC5p16ptLZRR-jud5J-ubfosJ9PDLzklUPDS2PiEWT4130_assertion description "[However, when individuals were stratified separately by NAT2 polymorphism (NAT2*5, NAT2*6, and NAT2*7), those who were heterozygous at the mutant locus NAT2*7 after adjustment for the NAT2 mutant loci NAT2*5 and NAT2*6 had a significantly higher risk of CRC (hazard ratio, 2.96; P = 0.012) and all of the cancers (hazard ratio, 3.37; P = 0.00004) than individuals homozygous for wild type at the NAT2*7 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53996.RApC5p16ptLZRR-jud5J-ubfosJ9PDLzklUPDS2PiEWT4130_provenance.
• NP53997.RAvJeq4ozJF-7ZueyQyGHgADs-bRlTOtvPUGWDGY38bsA130_assertion description "[The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53997.RAvJeq4ozJF-7ZueyQyGHgADs-bRlTOtvPUGWDGY38bsA130_provenance.
• NP54000.RAunhe0e9BlCAQgl4_Uo7fn6LXPtPLYqF9i0v3F0fxOvU130_assertion description "[ This study has identified a number of genes requiring further investigation including EPHX1, ADPRT1, CYP2D6, and AhR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54000.RAunhe0e9BlCAQgl4_Uo7fn6LXPtPLYqF9i0v3F0fxOvU130_provenance.
• NP54008.RAnYTeJceZ0IrlJPRtqCSlKFOUb-StmzhfukhYV3xNIcc130_assertion description "[The combined genotype of heterozygous arginine (Arg)/proline (Pro), Pro/Pro, and slow acetylator alleles of NAT2*5 and NAT2*6 showed higher, although not significant, risk of lung cancer compared with Arg/Arg and rapid acetylator alleles of NAT2*5 and NAT2*6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54008.RAnYTeJceZ0IrlJPRtqCSlKFOUb-StmzhfukhYV3xNIcc130_provenance.
• NP54010.RAtZnwITDENNilLVeaHAH_mRXiiFK4NoCynF68G9LnQaM130_assertion description "[Opposite effects of NAT2 gene polymorphisms on the risk of lung cancer are possible.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54010.RAtZnwITDENNilLVeaHAH_mRXiiFK4NoCynF68G9LnQaM130_provenance.
• NP54011.RApmmzguGki5aIUFlxCY6VHBgv0GXGihdgV3xoG9HOAz0130_assertion description "[As there is a recent meta-analysis of NAT2 studies on colon cancer (unlike in lung cancer), we have also undertaken a systematic review of NAT2 studies on lung cancer, and we incorporated our results in a meta-analysis consisting of 16 studies, 3,865 lung cancer patients and 6,077 control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54011.RApmmzguGki5aIUFlxCY6VHBgv0GXGihdgV3xoG9HOAz0130_provenance.
• NP54013.RAvvNP1CNmJVt9OQngzifdfpCGYMgGPZqm6B_6na-sZQg130_assertion description "[We have studied the influence of GSTM1 and NAT2 genotypes on aromatic DNA adduct level (AL) and HPRT mutant frequency (MF) in smokers with newly diagnosed lung cancer and matched population controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54013.RAvvNP1CNmJVt9OQngzifdfpCGYMgGPZqm6B_6na-sZQg130_provenance.
• NP54020.RAm7_tvzHd3ftBBhl0eVpxeIXztwTupJY9ZebyeW7t1DM130_assertion description "[These results suggest that there is no overall association between the NAT2 slow- or rapid-acetylation phenotype and breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54020.RAm7_tvzHd3ftBBhl0eVpxeIXztwTupJY9ZebyeW7t1DM130_provenance.
• NP54021.RAngrgJ-0kZ8Z5i5mvI_8Rlld70vK6CEML4_J8WBKZG9E130_assertion description "[In conclusion, our results provide support for the view that women who smoke and who have a genetically determined reduced inactivation of carcinogens (GSTM1 null genotype or slow NAT2 genotype (especially very slow NAT2 genotype)) are at increased risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54021.RAngrgJ-0kZ8Z5i5mvI_8Rlld70vK6CEML4_J8WBKZG9E130_provenance.
• NP54022.RAvoqSzthzzXXSQbPZOIiWAFq58P4-h5vjDyWOlFUxWyM130_assertion description "[Genetic polymorphisms in folate and alcohol metabolism and breast cancer risk: a case-control study in Thai women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54022.RAvoqSzthzzXXSQbPZOIiWAFq58P4-h5vjDyWOlFUxWyM130_provenance.
• NP54032.RAj972EzYWTymoiaItcV0itgqfJz-cQC8IW76zVUdNOBU130_assertion description "[Our study suggests that the NAT2 slow acetylators may be a determinant in susceptibility to asthma disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54032.RAj972EzYWTymoiaItcV0itgqfJz-cQC8IW76zVUdNOBU130_provenance.
• NP54034.RAqxZDhGtR9xyMMfc6RcWO4KPa78Z5-SpByWo8JBwMcHc130_assertion description "[While, in non-smokers patients the slow NAT2 did not appear to influence bladder cancer susceptibility; our results suggested that it might act with an additive contribution with tobacco as well as with that determined by MTR 2756 AG or 2756 GG genotypes (p = 0.0008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54034.RAqxZDhGtR9xyMMfc6RcWO4KPa78Z5-SpByWo8JBwMcHc130_provenance.
• NP54048.RAuUMQrwkd2yDKRP8SzUxPMTukZN9fWMGxKJgB1moxCxQ130_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." NP54048.RAuUMQrwkd2yDKRP8SzUxPMTukZN9fWMGxKJgB1moxCxQ130_provenance.

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