Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP55626.RApWicfwr2BEpg9r8fEVjrA8l-wVQUaAT6_0FP3dSiALQ130_assertion description "[This study demonstrates the frequency of this cSNP complies well with the Hardy-Weinberg equilibrium in normal group,T418M(C/T) is only a polymorphic maker of KCNA7 gene,and the possibility of association between NIDDM and KCNA7 can not be excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55626.RApWicfwr2BEpg9r8fEVjrA8l-wVQUaAT6_0FP3dSiALQ130_provenance.
- NP55631.RAjLnTunjuVtrctZYO9IlIOYC0PsfaFXySQcdh9nmAcZU130_assertion description "[V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55631.RAjLnTunjuVtrctZYO9IlIOYC0PsfaFXySQcdh9nmAcZU130_provenance.
- NP55632.RAgz-wVgWUHusP8lJUoByYjquMrne8-qcRL5sTWN6F8N0130_assertion description "[a low JAK2V617F allele burden at diagnosis is preferentially associated with a myelodepletive rather than myeloproliferative phenotype and represents an independent factor associated with shortened survival in patients with PMF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55632.RAgz-wVgWUHusP8lJUoByYjquMrne8-qcRL5sTWN6F8N0130_provenance.
- NP55634.RAlh9V8u2zeuy-auWBGWIjFiYyYl9CCWZYOJQGvLCo5vE130_assertion description "[Frequency and clinical correlates of JAK2 46/1 (GGCC) haplotype in primary myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55634.RAlh9V8u2zeuy-auWBGWIjFiYyYl9CCWZYOJQGvLCo5vE130_provenance.
- NP55636.RAi6BJyv4mMie_EQDRF7hwA1047o2CE5zKg_fPrGKuIKU130_assertion description "[Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55636.RAi6BJyv4mMie_EQDRF7hwA1047o2CE5zKg_fPrGKuIKU130_provenance.
- NP55639.RAt-ffZM1u8HeI2fm8GLyMl2kWO0scnr6u4bu50HZXETA130_assertion description "[A novel JAK2 exon 12 mutation identified in the retrospective analysis of paraffin-embedded tissues of polycythemia vera patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55639.RAt-ffZM1u8HeI2fm8GLyMl2kWO0scnr6u4bu50HZXETA130_provenance.
- NP55644.RAmPdPc0uXyiwiGX6QumyEpXVbI4WsSoJpZcKQO9RAjAM130_assertion description "[More than 90% of individuals with a JAG1 mutation or AGS have cardiovascular anomalies, with branch PA stenosis the most common abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55644.RAmPdPc0uXyiwiGX6QumyEpXVbI4WsSoJpZcKQO9RAjAM130_provenance.
- NP55645.RAqw0Clo72VmV_bVSqDTMFejyPSWm-_KtuWc1qH1iEje0130_assertion description "[In conclusion, this pilot identified SNPs as potential markers that could predict hepatitis B patient response. These observations may help guide future large-scale studies in examining host SNPs for their clinical utility in predicting IFN response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55645.RAqw0Clo72VmV_bVSqDTMFejyPSWm-_KtuWc1qH1iEje0130_provenance.
- NP55647.RAqIA3mwNVJyKvUxQ_hLUeeH_zd9UV4KXNMSuQSiqJ8Dg130_assertion description "[Polymorphism in the ITPA gene predicts AZA intolerance. Alternative immunosuppressive drugs, particularly 6-thioguanine, should be considered for AZA-intolerant patients with ITPase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55647.RAqIA3mwNVJyKvUxQ_hLUeeH_zd9UV4KXNMSuQSiqJ8Dg130_provenance.
- NP55656.RAjzkw6OhAGrh_J-KmAxT4EFCYRCaTtbB61QDGznEBct8130_assertion description "[Role of five platelet membrane glycoprotein polymorphisms in branch retinal vein occlusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55656.RAjzkw6OhAGrh_J-KmAxT4EFCYRCaTtbB61QDGznEBct8130_provenance.
- NP55657.RAvo0IjTzlvydYTKmnxCZIPRNb0wqnIuNQseE8GE1XO6E130_assertion description "[Thus, genetic polymorphisms may be associated with subsequent myocardial infarction, and may also be associated with treatment-associated bleeding among coronary patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55657.RAvo0IjTzlvydYTKmnxCZIPRNb0wqnIuNQseE8GE1XO6E130_provenance.
- NP55669.RAsOc_v1MJvKgzPvfdWyWOgg9gzSLY_Ty5Q2k-nFu7zn0130_assertion description "[High loading dose of clopidogrel is unable to satisfactorily inhibit platelet reactivity in patients with glycoprotein IIIA gene polymorphism: a genetic substudy of PRAGUE-8 trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55669.RAsOc_v1MJvKgzPvfdWyWOgg9gzSLY_Ty5Q2k-nFu7zn0130_provenance.
- NP55671.RAv14SE9qruVvBlAvbnkUCNR7kNYYFKaPGIoamYSBaYC0130_assertion description "[In CAD patients receiving daily low dose of aspirin, there is a significant and independent association between the expression of GPIIIa PlA1 allele and the occurrence of persistent HPR detected with PFA-100.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55671.RAv14SE9qruVvBlAvbnkUCNR7kNYYFKaPGIoamYSBaYC0130_provenance.
- NP55672.RAusMedmOnQEx5b_AN_ZayUd8ag_WP4CRznzLH-gbnK1c130_assertion description "[The glycoprotein IIb/IIIa genotype was not shown to indicate the presence of atherosclerotic plaque. There was no correlation between the genotype and plaque vulnerability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55672.RAusMedmOnQEx5b_AN_ZayUd8ag_WP4CRznzLH-gbnK1c130_provenance.
- NP55674.RAiiBloFQe6miRDKN345QkGIq82q0ZKBMLuNYQ8jiz8-g130_assertion description "[Genetic polymorphisms of clotting factors and coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55674.RAiiBloFQe6miRDKN345QkGIq82q0ZKBMLuNYQ8jiz8-g130_provenance.
- NP55678.RAomQbhJ5oE-LRbRdnI0S8vTy1mqwyEMSOKCTRhmn3KqU130_assertion description "[ Our results suggest that these polymorphisms play a minor role in PIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55678.RAomQbhJ5oE-LRbRdnI0S8vTy1mqwyEMSOKCTRhmn3KqU130_provenance.
- NP55682.RAvCSNxyD0Ym-GdqM9IbIecNmcFRxWWzk0DwN_QAbWgDo130_assertion description "[ Our results did not show the causative relationship between the existence of platelets GP IIIa/GP Ia mutations and venous system thrombosis in the women in labor. Probably presence of pro-thrombotic mutations of platelets glycoprotein in this group of patients does not represent the increased risk of thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55682.RAvCSNxyD0Ym-GdqM9IbIecNmcFRxWWzk0DwN_QAbWgDo130_provenance.
- NP55683.RAkfYwi51PhTeoB4SpvMCiTbH9ujU6MvDxJR-Qwny77Rc130_assertion description "[Prevalence of prothrombotic polymorphisms in Greece.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55683.RAkfYwi51PhTeoB4SpvMCiTbH9ujU6MvDxJR-Qwny77Rc130_provenance.
- NP55688.RApWGYywYdO0w4HVJ7Xk38l6dhUwJve3DhvKGWN43YfI8130_assertion description "[PIA1/A2 polymorphism of the platelet glycoprotein receptor IIb/IIIIa and its correlation with myocardial infarction: an appraisal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55688.RApWGYywYdO0w4HVJ7Xk38l6dhUwJve3DhvKGWN43YfI8130_provenance.
- NP55696.RAvp8BpM5gCYi_yOwueGvgU56R9M0KPY0flDJeeGIci1g130_assertion description "[Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55696.RAvp8BpM5gCYi_yOwueGvgU56R9M0KPY0flDJeeGIci1g130_provenance.
- NP55701.RAukd3quFhmUQL5cG0Sn7CkV34OSPQtuSjmF2Qpkp4kzg130_assertion description "[ A2 allele of the GpIIIa gene is an independent risk factor for LVD stroke in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55701.RAukd3quFhmUQL5cG0Sn7CkV34OSPQtuSjmF2Qpkp4kzg130_provenance.
- NP55704.RAmNIBgvgRqjx5H2qiL0kL5kZqsI7evjJXYlt4WJpTYkg130_assertion description "[Certain genetic polymorphisms of coagulation system could result unfavorable haemorheological changes, however non of them increases the mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55704.RAmNIBgvgRqjx5H2qiL0kL5kZqsI7evjJXYlt4WJpTYkg130_provenance.
- NP55711.RAlDQwER6CjR3g-fyy94jeRa5sFFWvnBdkh51Dif7H6Qo130_assertion description "[ There is a significant reduction in the P1(A2) polymorphism in smokers admitted with non-ST-elevation ACS compared with nonsmokers, which suggests an interaction between smoking and this polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55711.RAlDQwER6CjR3g-fyy94jeRa5sFFWvnBdkh51Dif7H6Qo130_provenance.
- NP55712.RAi9olcJHtN_z3oQmcY19jnHJssWPNByIy-Gj0-BYkrtg130_assertion description "[The laboratory phenomenon of clopidogrel resistance exists. Large multicenter studies of this issue are needed to identify simple and least expensive resistance methods and clear diagnostic criteria that enable the findings to be compared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55712.RAi9olcJHtN_z3oQmcY19jnHJssWPNByIy-Gj0-BYkrtg130_provenance.
- NP55714.RAiklqnykMBl3_mjIhFkxhzq0CvHJqWCAmccbFUpn9WOA130_assertion description "[Platelet GPIIb/IIIa (P1A 1/2) polymorphism in SLE: clinical and laboratory association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55714.RAiklqnykMBl3_mjIhFkxhzq0CvHJqWCAmccbFUpn9WOA130_provenance.
- NP55715.RAgw2Koew2NE_oH62z1cizu3802tBB7idLCwjPXBeb2_o130_assertion description "[Our results emphasize the need to account for complex multi-gene influences and interactions when assessing the molecular pathology of multifactorial medical entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55715.RAgw2Koew2NE_oH62z1cizu3802tBB7idLCwjPXBeb2_o130_provenance.
- NP55717.RAvYGwNw3tRokMLlekd9r6jHD7f7TEBzWgL6FbJ6M-jAg130_assertion description "[In this large, prospective study, we found little evidence that the two previously described polymorphisms in the CD14 and CD18 genes are associated with risks of future stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55717.RAvYGwNw3tRokMLlekd9r6jHD7f7TEBzWgL6FbJ6M-jAg130_provenance.
- NP55724.RAs2o644wCrsZenwjudRXQUj1IgtHvMW44c_HSJX5ls0E130_assertion description "[None of these variants led to amino acid (AA) substitutions. Interestingly, homozygosity of the new variant 269A was not found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55724.RAs2o644wCrsZenwjudRXQUj1IgtHvMW44c_HSJX5ls0E130_provenance.
- NP55732.RAuJzAMqpmqm1EKx_waf5CcXoAxSsSj7L8j7RyQby6xD0130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55732.RAuJzAMqpmqm1EKx_waf5CcXoAxSsSj7L8j7RyQby6xD0130_provenance.
- NP55737.RAuCJqNIqWmMegnyisRnwUwqB-8uqBUwtoCxz4bFPpMZU130_assertion description "[These data suggest an underlying prothrombotic state, but do not support the polymorphisms studied as risk factors for thrombotic stroke in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55737.RAuCJqNIqWmMegnyisRnwUwqB-8uqBUwtoCxz4bFPpMZU130_provenance.
- NP55739.RArMDpDBNdNGzqtAMIY9v9F02IQCqvw-wS9mIQT_qErW0130_assertion description "[This finding seems to support the hypothesis of a real role of this polymorphism in the risk of events in patients with CAD]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55739.RArMDpDBNdNGzqtAMIY9v9F02IQCqvw-wS9mIQT_qErW0130_provenance.
- NP55740.RAszARrDNOTruBxI1HWahEeV-EVkKbk1hAnPhuGsKWiNw130_assertion description "[Platelet glycoprotein IIb/IIIa genetic polymorphism is associated with plasma fibrinogen levels in myocardial infarction patients. The REGICOR Investigators.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55740.RAszARrDNOTruBxI1HWahEeV-EVkKbk1hAnPhuGsKWiNw130_provenance.
- NP55745.RAlBCbniNjvx5VDwuGVKY1vD_5A56kRJnv5WPIUB5DuSY130_assertion description "[Relationship between platelet activation related factors and polymorphism of related genes in patients with coronary heart disease of blood-stasis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55745.RAlBCbniNjvx5VDwuGVKY1vD_5A56kRJnv5WPIUB5DuSY130_provenance.
- NP55749.RAlZ0gX03MDEpKsJrg59vWRW_xyh8_P8lhEu38lrM6UwI130_assertion description "[Role of five platelet membrane glycoprotein polymorphisms in branch retinal vein occlusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55749.RAlZ0gX03MDEpKsJrg59vWRW_xyh8_P8lhEu38lrM6UwI130_provenance.
- NP55750.RAoN83_eEgKkM2LZbES-zl6NZs89jaLcFusgcBa6vFKGw130_assertion description "[ The L34 allele of the amino acid polymorphism of the FXIII gene is associated with a decreased risk of AMI, and this protecting association seems to be more pronounced in smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55750.RAoN83_eEgKkM2LZbES-zl6NZs89jaLcFusgcBa6vFKGw130_provenance.
- NP55755.RAuE7wG4OWkiO6uak0BxAGCHqj8ZDhx1rnIQvJSbJvqhw130_assertion description "[Association of the platelet glycoprotein Ia C807T gene polymorphism with nonfatal myocardial infarction in younger patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55755.RAuE7wG4OWkiO6uak0BxAGCHqj8ZDhx1rnIQvJSbJvqhw130_provenance.
- NP55758.RAt2p2uv1thhzRK_pGc_T4Y99aDDxLGI-_eZcenQAEjEE130_assertion description "[In conclusion, platelet GP Ia C807T and GP Ib C3550T polymorphisms in our population are less common compared with Caucasians, and GP IIIa Pl(A1/A2) genetic mutation is not found, and all of them are not associated with ischemic stroke in young Taiwanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55758.RAt2p2uv1thhzRK_pGc_T4Y99aDDxLGI-_eZcenQAEjEE130_provenance.
- NP55763.RAmKW-JJjr3xi7Q9P3KZ4m1fH-TZTwAPQNnmE2nKXAFh0130_assertion description "[Genetic polymorphisms of platelet adhesive molecules: association with breast cancer risk and clinical presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55763.RAmKW-JJjr3xi7Q9P3KZ4m1fH-TZTwAPQNnmE2nKXAFh0130_provenance.
- NP55768.RAi0r3mFwvHWSb-0dk_vbHYYnU2Ha0y27Pn7CHxX1qjkU130_assertion description "[These results suggest that the number of 807T alleles in alpha2 integrin is protective against atherosclerotic arterial wall thickening and the occurrence of plaque in patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55768.RAi0r3mFwvHWSb-0dk_vbHYYnU2Ha0y27Pn7CHxX1qjkU130_provenance.
- NP55769.RAhDNoMJYxn845yuuNiU4YZ_qcR35OKa8-DWU5T85mNPM130_assertion description "[A case-control study was performed to study the genetic association between DR and polymorphic variants of EDN1 (Lys198Asn), LTA (IVS1-80C>A, IVS1-206G>C, IVS1-252A>G), eNOS (Glu298Asp), and ITGA2 (BgI II) in a Chinese population with type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55769.RAhDNoMJYxn845yuuNiU4YZ_qcR35OKa8-DWU5T85mNPM130_provenance.
- NP55771.RAgIdpeT8npPL6zHXopMOfpnitKH7E968PKWyPWbgKH4g130_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." NP55771.RAgIdpeT8npPL6zHXopMOfpnitKH7E968PKWyPWbgKH4g130_provenance.
- NP55781.RAmq1ow6i4etzECMDe5KWqY4njL3MYWtMVqCYd5Uzj6So130_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." NP55781.RAmq1ow6i4etzECMDe5KWqY4njL3MYWtMVqCYd5Uzj6So130_provenance.
- NP55786.RAtnDYG2UHcHolLMafUoYiN9_PNF04zitvY1xxzUkQ6pI130_assertion description "[These data indicate that IRS2 is an influential gene in severe obesity and glucose intolerance in this population, whereas gene-based haplotypes of IRS2 have revealed heterogeneity in the behaviour of the Gly1057Asp mutation in relation to insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55786.RAtnDYG2UHcHolLMafUoYiN9_PNF04zitvY1xxzUkQ6pI130_provenance.
- NP55788.RArJucprpQRDzqtUMigWpCISaRwyb4p2NuCLI61b3w794130_assertion description "[In Asian Indians, the DD genotype increases susceptibility to type 2 diabetes by interacting with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55788.RArJucprpQRDzqtUMigWpCISaRwyb4p2NuCLI61b3w794130_provenance.
- NP55789.RAgGdH06L2keU-i4Bu47Z0BtP1ynbegJ-lBNdHvUQoe9M130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55789.RAgGdH06L2keU-i4Bu47Z0BtP1ynbegJ-lBNdHvUQoe9M130_provenance.
- NP55794.RAsAI6upwmU8KDIa4poap9tAtXaDV3zuUyillTg2sHQdo130_assertion description "[We hypothesized that functional polymorphisms in the insulin pathway genes INS, INSR, IGFBPI, insulin receptor substrate 1 (IRS1), and IRS2 may be associated with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55794.RAsAI6upwmU8KDIa4poap9tAtXaDV3zuUyillTg2sHQdo130_provenance.
- NP55795.RAsSXIMpU6ZrlsAl09v14I989BkwpdROWT26ZaPt8z8UI130_assertion description "[ These results support a role of the insulin and/or insulin-like growth factor pathways in the etiology of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55795.RAsSXIMpU6ZrlsAl09v14I989BkwpdROWT26ZaPt8z8UI130_provenance.
- NP55797.RAmEoUg35dqIssDFSKcKS3EOhv9B-9HfWwBd4RnrQ6S2s130_assertion description "[No significant association of PPARG, PGC1, IRS1, KCNJ11 and TCF7L2 gene polymorphisms and the age at diagnosis of T2DM was observed in the present study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55797.RAmEoUg35dqIssDFSKcKS3EOhv9B-9HfWwBd4RnrQ6S2s130_provenance.
- NP55799.RAmGatUbZ_x-TTKIsfC1pSaUG9vVVqnBiHraGENqKtU08130_assertion description "[The association of the polymorphisms Gly972Arg, SNP43, and Pro12Ala, of the genes IRS1, CAPN10, PPARG2, with the risk of failure to sulphonylurea and metformin therapies was determinated in patients with DT2 in Yucatn, Mxico.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55799.RAmGatUbZ_x-TTKIsfC1pSaUG9vVVqnBiHraGENqKtU08130_provenance.
- NP55814.RAkevB56_okn5utWjebdGKJGOzyFbHzeIPfhGGlLyE7nc130_assertion description "[These results suggest that the IRS-2 Gly(1057)Asp polymorphism influences blood glucose levels in nondiabetic white and African-American women with PCOS. Thus, individuals with the common IRS-2 Gly/Gly genotype may be at increased risk of developing type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55814.RAkevB56_okn5utWjebdGKJGOzyFbHzeIPfhGGlLyE7nc130_provenance.
- NP55816.RAl-sPixPRDFfszO6IpLZI9ce76vadco-byUlHjIJjbhc130_assertion description "[No association between common Gly972Arg variant of the insulin receptor substrate-1 and polycystic ovary syndrome in Southern Chilean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55816.RAl-sPixPRDFfszO6IpLZI9ce76vadco-byUlHjIJjbhc130_provenance.
- NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion description "[ While subtle effects of these variants cannot be excluded in this system, it is unlikely that these variants are responsible for the extreme insulin resistance seen in the subjects harbouring them. Although IRS proteins play a central role in insulin signalling, functionally significant mutations in the IRS-1 gene are a rare cause of human syndromes of severe insulin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance.
- NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score can improve the predictive capacity or the risk classification of classical risk functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55819.RAofXSZ-DDeQomIV0fs4SMIPOyaM00oYIPoUzMCO4kds8130_provenance.
- NP55820.RAlbZphlHlAmt1HElgYqwrEsiJ6pSf3nTEsZxugMY71Sk130_assertion description "[Relationship between polymorphism of IRF-3 gene codon 427 and esophageal cancer in Anyang population of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55820.RAlbZphlHlAmt1HElgYqwrEsiJ6pSf3nTEsZxugMY71Sk130_provenance.
- NP55824.RAkTPOD623qqMutm3jpfQ3E4YsyfThRRt-mwGzbNeE6yk130_assertion description "[Recently, two studies provided convincing evidence that IFN regulatory factor 5 (IRF5) gene polymorphisms are significantly associated with systemic lupus erythematosus (SLE) in several white populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55824.RAkTPOD623qqMutm3jpfQ3E4YsyfThRRt-mwGzbNeE6yk130_provenance.
- NP55829.RAhHE5vBSkjCr6hqysioGWFAiKtpvIvn-ez8wRCYXQVDY130_assertion description "[Mutation and association analysis of the interferon regulatory factor 2 gene (IRF2) with atopic dermatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55829.RAhHE5vBSkjCr6hqysioGWFAiKtpvIvn-ez8wRCYXQVDY130_provenance.
- NP55831.RAjca7JlUkck1SGfydJrO0fKlXaJG97LZ_EJCsFmGis_0130_assertion description "[These findings provide strong evidence of which IFN-gamma CA repeat and IRF-1 GT repeat polymorphisms influence the risk of asthma for children in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55831.RAjca7JlUkck1SGfydJrO0fKlXaJG97LZ_EJCsFmGis_0130_provenance.
- NP55836.RAvXN50t3LzaLjYmGrAOtHp_NvvFQ7SZWnyurGOhIjUQs130_assertion description "[A significant association between JIA and a polymorphism in the interferon regulatory factor 1 (IRF-1) gene has previously been reported, implicating IRF1 in disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55836.RAvXN50t3LzaLjYmGrAOtHp_NvvFQ7SZWnyurGOhIjUQs130_provenance.
- NP55837.RAgHydW2Mk8zI0fp3uBHiZG-XRb2aQUM6wz6RUqj42pF0130_assertion description "[ We found that the level of education, the age at first intercourse, and the number of children were independent risk factors in cervix carcinogenesis. The specific combinations of p53, p21, and IRF-1 gene-gene and gene-environmental interactions were significantly noted in the cervix carcinogenesis of Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55837.RAgHydW2Mk8zI0fp3uBHiZG-XRb2aQUM6wz6RUqj42pF0130_provenance.
- NP55839.RAlx7ipF-qi5w71QVTAnjFs0Q4N48DL7j2qvGmfVQid78130_assertion description "[These results suggest that IRF-1 promoter polymorphisms may contribute, at least partially, to host antiviral activity for chronic hepatitis C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55839.RAlx7ipF-qi5w71QVTAnjFs0Q4N48DL7j2qvGmfVQid78130_provenance.
- NP55844.RAg3l5zGY9990utsMQRxdU5C7jTVMicWHfh7GT8wygnsE130_assertion description "[We have observed a combined prevalence of missense variants in the coding region of the IPF-1 gene of around 1%, in unselected patients with the common form of late-onset type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55844.RAg3l5zGY9990utsMQRxdU5C7jTVMicWHfh7GT8wygnsE130_provenance.
- NP55846.RAoErtabrnqzhVU6IZ6E7SnW0VePCXzhE6xWRwk62W5TM130_assertion description "[Insulin Promoter Factor 1 variation is associated with type 2 diabetes in African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55846.RAoErtabrnqzhVU6IZ6E7SnW0VePCXzhE6xWRwk62W5TM130_provenance.
- NP55848.RAlZVLUQhR0aiENoalzuV2rSChjdoMUlA6bdOAV0LNjlI130_assertion description "[We conclude that D76N IPF1 is not contributing to T2D in early-onset or late-onset cohorts in the currently present worldwide dataset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55848.RAlZVLUQhR0aiENoalzuV2rSChjdoMUlA6bdOAV0LNjlI130_provenance.
- NP55858.RAtZZq6ZfTfXyEq9T0EfM-w66FgeztW78dszsAlpvbdQU130_assertion description "[Genotypes identified by two restriction fragment length polymorphisms (RFLPs) of the insulin receptor gene (IRG) with the restriction endonuclease Sst-1 were determined in a Japanese group comprising 51 patients with non-insulin-dependent diabetes mellitus (NIDDM) and 50 control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55858.RAtZZq6ZfTfXyEq9T0EfM-w66FgeztW78dszsAlpvbdQU130_provenance.
- NP55865.RAhIsJNbnZMq1UPahxvZekJCL6QUbfqKIoQvaH2ZEp9Us130_assertion description "[(2) The 1058 site nucleotide polymorphism of insulin receptor gene is one of the susceptibility genes in patients with PCOS, especially in non-obese PCOS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55865.RAhIsJNbnZMq1UPahxvZekJCL6QUbfqKIoQvaH2ZEp9Us130_provenance.
- NP55868.RAh1MaffQoZccRqvc9u8MStEojlnp9fQwZEDoVNUOuJFg130_assertion description "[ No significant association between A1166C molecular variant of AT1R gene and insulin resistance was found in Chinese with CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55868.RAh1MaffQoZccRqvc9u8MStEojlnp9fQwZEDoVNUOuJFg130_provenance.
- NP55871.RAm5TgbDkOV4mMFiMb_ZAjr0o0A4ornNAP-NDhYLOHMiw130_assertion description "[Human diabetes associated with a deletion of the tyrosine kinase domain of the insulin receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55871.RAm5TgbDkOV4mMFiMb_ZAjr0o0A4ornNAP-NDhYLOHMiw130_provenance.
- NP55880.RAiND8viK_voGFWqlvj8AkSQg2ZQLDH0M1_jRXftweW_c130_assertion description "[A systematic search for single nucleotide polymorphisms (SNPs) in the insulin receptor gene: association of an SNP with hyperlipidemia in Japanese type 2 diabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55880.RAiND8viK_voGFWqlvj8AkSQg2ZQLDH0M1_jRXftweW_c130_provenance.
- NP55882.RAghUExDn4E7GtPTzU5aD9DlG4GwfrwJfs-Ln-hY5QGYs130_assertion description "[Insulin-resistant diabetes associated with partial deletion of insulin-receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55882.RAghUExDn4E7GtPTzU5aD9DlG4GwfrwJfs-Ln-hY5QGYs130_provenance.
- NP55883.RAn_IrUVTH53-JJ8rtStnoDBPZUVkjXNdtHwkzULT9TsI130_assertion description "[Insulin-like 3/relaxin-like factor gene mutations are associated with cryptorchidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55883.RAn_IrUVTH53-JJ8rtStnoDBPZUVkjXNdtHwkzULT9TsI130_provenance.
- NP55885.RAjFtGb26VPouvDhTFwRMvDCbOp5iPQ6_apdCKlIFKIRA130_assertion description "[Novel mutations involving the INSL3 gene associated with cryptorchidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55885.RAjFtGb26VPouvDhTFwRMvDCbOp5iPQ6_apdCKlIFKIRA130_provenance.
- NP55889.RAjv8nGuTUab6zFRX-NgoQhHXfWWTl-vV8vCBLL9yExVA130_assertion description "[The polymorphism of INS may play a role in the aetiology of prostate cancer. Given the high prevalence of the CC genotype and its association with late age of onset of low-grade tumours, this polymorphism may contribute to the unique characteristics of prostate cancer, namely a high prevalence of indolent cancers and the dramatic increase in incidence with age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55889.RAjv8nGuTUab6zFRX-NgoQhHXfWWTl-vV8vCBLL9yExVA130_provenance.
- NP55890.RAiDh_wwSztSILfbwS3XpcFXBwe7hQw-bMYSBuoRH2v6U130_assertion description "[ These results support a role of the insulin and/or insulin-like growth factor pathways in the etiology of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55890.RAiDh_wwSztSILfbwS3XpcFXBwe7hQw-bMYSBuoRH2v6U130_provenance.
- NP55899.RAtSlwTBUEV2wngMKM-wPipIIdjbBFqu_I7tXnNKwp6Lw130_assertion description "[It is concluded that DNA marker flanking the insulin gene may not be associated with the development of NIDDM in Chinese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55899.RAtSlwTBUEV2wngMKM-wPipIIdjbBFqu_I7tXnNKwp6Lw130_provenance.
- NP55904.RAgCXA2T_NbC-Ln66TGiv1L28Rs2Wb_bZJYat2p9FSt3s130_assertion description "[Non-insulin-dependent diabetes mellitus and the 5' hypervariable region of the insulin gene in two South African Indian families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55904.RAgCXA2T_NbC-Ln66TGiv1L28Rs2Wb_bZJYat2p9FSt3s130_provenance.
- NP55905.RAiWRT08dfxkm4DAWuqG9UL8pof0ob0VHHJeU0Jpyqfeo130_assertion description "[INS VNTR class genotype and indexes of body size and obesity: population-based studies of 7,999 middle-aged men and women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55905.RAiWRT08dfxkm4DAWuqG9UL8pof0ob0VHHJeU0Jpyqfeo130_provenance.
- NP55906.RAhXEZHhJoH3ULnIOsFbC4dJA_s1kca7hesooPuk0F1Xs130_assertion description "[The INS VNTR can therefore be considered a quantitative trait locus influencing glucose-stimulated insulin physiology in obese juveniles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55906.RAhXEZHhJoH3ULnIOsFbC4dJA_s1kca7hesooPuk0F1Xs130_provenance.
- NP55916.RAgkZq1hRgVgrXGlY6zzJnzY7Rah2b6GFYv9cvgcFWA_k130_assertion description "[Multiple DNA variant association analysis: application to the insulin gene region in type I diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55916.RAgkZq1hRgVgrXGlY6zzJnzY7Rah2b6GFYv9cvgcFWA_k130_provenance.
- NP55918.RApjxifbMW7mcv0Q94OsBNWLOs2fMRZlDslY2Gf3UE9E8130_assertion description "[A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55918.RApjxifbMW7mcv0Q94OsBNWLOs2fMRZlDslY2Gf3UE9E8130_provenance.
- NP55919.RAh--AgdvSPglrdweVacTIDnEyT-xZm-3r281hgXUnCck130_assertion description "[Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55919.RAh--AgdvSPglrdweVacTIDnEyT-xZm-3r281hgXUnCck130_provenance.
- NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_assertion description "[INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55921.RAkGDhk3uM4FD7AKAZ8dI1aPKuO-O_Sqb2aqA03mmW3ng130_provenance.
- NP55929.RAjSAH0hLhIMLntEHmpPhdPvFc389b_ZzruZ8V7lz-5Lw130_assertion description "[ Our results indicate that -16C>T and 769G>A variants in INHalpha gene may not be associated to POF disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55929.RAjSAH0hLhIMLntEHmpPhdPvFc389b_ZzruZ8V7lz-5Lw130_provenance.
- NP55935.RAn8z4XdCUmQ7F5U1jSnbcIfPvfDGtPkTEExfhu-4EcI8130_assertion description "[To determine whether variants in the promoter region of the inhibin alpha gene (INHA) are associated with premature ovarian failure (POF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55935.RAn8z4XdCUmQ7F5U1jSnbcIfPvfDGtPkTEExfhu-4EcI8130_provenance.
- NP55939.RAhX1s-Z6b9kB8ledMVlqvshqgaQVwF0NK2eISL4tN634130_assertion description "[These findings suggest that mutations of the IMPDH1 gene cause ADRP in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55939.RAhX1s-Z6b9kB8ledMVlqvshqgaQVwF0NK2eISL4tN634130_provenance.
- NP55942.RAk9GYhLHtWjSTAFNue_-FCJLFuFDL0KgAHJVOTpDDROo130_assertion description "[The IL9R region contribution in asthma is supported by genetic association in an isolated population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55942.RAk9GYhLHtWjSTAFNue_-FCJLFuFDL0KgAHJVOTpDDROo130_provenance.
- NP55948.RAqIBo5aPu01u_BwF60DTNsSxG2qdER82mmPLWVDfBNv4130_assertion description "[Variants in the IL4RA gene alone may not exert any major influence on susceptibility to asthma-related diseases in childhood, but in combination with other genes, such as IL9R, IL4RA may be an important gene for disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55948.RAqIBo5aPu01u_BwF60DTNsSxG2qdER82mmPLWVDfBNv4130_provenance.
- NP55953.RAnBbt0HgLYHOSoguX_w8WW_EZgKIcIG9HY-moB9zJMxw130_assertion description "[These data suggest that IL-8 is important in the genetic control of human TB susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55953.RAnBbt0HgLYHOSoguX_w8WW_EZgKIcIG9HY-moB9zJMxw130_provenance.
- NP55954.RAglBRwrrdQ8DNQpIc2Sls_2UpufZ2RjL7IQ59PNT54dE130_assertion description "[Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55954.RAglBRwrrdQ8DNQpIc2Sls_2UpufZ2RjL7IQ59PNT54dE130_provenance.
- NP55955.RAmk4GH709lozIUeuhYDZoX2kj6SKBtBypDLQ2MGYnI7g130_assertion description "[The current study does not demonstrate an association between CD14 (-260) polymorphism and AD, neither through an independent effect nor through interaction with APOE varepsilon4 allele or interleukin (IL)-1A, IL-6, IL-8, tumor necrosis factor (TNF)-alpha, and intercellular adhesion molecule-1 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55955.RAmk4GH709lozIUeuhYDZoX2kj6SKBtBypDLQ2MGYnI7g130_provenance.
- NP55957.RAjO_89QZG02-qPADpvZGlsbFAowHUkq1OBwx4JMWJ6w4130_assertion description "[Results: The presence of the MTHFR 677 C/T and 677 T/T genotypes conferred a marginally significant increase in the risk for AD (OR = 1.666, 95% CI = 1.022-2.715, and OR = 1.892, 95% CI = 1.124-3.187) and the presence of the IL-8 -251 polymorphism was not associated with AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55957.RAjO_89QZG02-qPADpvZGlsbFAowHUkq1OBwx4JMWJ6w4130_provenance.
- NP55959.RAkIe4Xw_yCw1FR-s48IBsqcJOo9-Ba5rSiV_p-JjsNk8130_assertion description "[We argue that different caste populations from the same geographic location can be pooled for the purpose of population association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55959.RAkIe4Xw_yCw1FR-s48IBsqcJOo9-Ba5rSiV_p-JjsNk8130_provenance.
- NP55962.RAokT2TwY4Gv6jweJZN1y7ilrmtdo-t780ghhBGxI04Xs130_assertion description "[correlations of the TGF-beta1 and IL-8 single nucleotide polymorphisms (SNPs) with chronic pancreatitis underline the importance of these cytokines in the pathomechanism of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55962.RAokT2TwY4Gv6jweJZN1y7ilrmtdo-t780ghhBGxI04Xs130_provenance.
- NP55963.RAiZ1kndPgeGoGGQ4TwNyeTYutPozZuU11PYXOi_pWuYs130_assertion description "[A total of 144 female breast cancer patients and 263 cancer-free population controls were genotyped for the interleukin (IL)-1beta-511 (T/C), IL-6 -174 (G/C), tumour necrosis factor (TNF)-alpha-308 (A/G), IL-10 -1082 (A/G), IL-8 -251 (A/T) and vascular endothelial growth factor (VEGF) -1154 (A/G) SNPs, using amplification refractory mutation system polymerase chain reaction (ARMS-PCR) and TaqMan (Applied Biosystems, Foster City, CA, USA) 5' nuclease assays for allelic discrimination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55963.RAiZ1kndPgeGoGGQ4TwNyeTYutPozZuU11PYXOi_pWuYs130_provenance.
- NP55964.RAkihPWIaBQ7BC6dvYSvcJKRC0HwykSIpuUOHk8Hfb-sg130_assertion description "[Genetic variation in IL-8 associated with increased risk and poor prognosis of breast carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55964.RAkihPWIaBQ7BC6dvYSvcJKRC0HwykSIpuUOHk8Hfb-sg130_provenance.
- NP55965.RAn0CwKTboBNtYGhCRVdKVpJvqB0W3H2u4Ihy2HpE8eJA130_assertion description "[Peroxisome proliferator-activated corrected receptor-gamma2 corrected Pro12Ala, interaction with alcohol intake and NSAID use, in relation to risk of breast cancer in a prospective study of Danes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55965.RAn0CwKTboBNtYGhCRVdKVpJvqB0W3H2u4Ihy2HpE8eJA130_provenance.
- NP55972.RAhhDDM-wGUIKicTUb9Ro7KK09sh_aCtprXIJgzYXgIow130_assertion description "[ The IL-8 -251T allele is significantly associated with increased risk of gastric carcinoma, particularly the diffuse and mixed types in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55972.RAhhDDM-wGUIKicTUb9Ro7KK09sh_aCtprXIJgzYXgIow130_provenance.
- NP55986.RAqMFpYDQXMWfZwhevtnRX6an0bkpXf4dIBLZ9zm5E2jc130_assertion description "[We found that sequence variants in inflammatory genes interact with plasma antioxidants to modulate prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55986.RAqMFpYDQXMWfZwhevtnRX6an0bkpXf4dIBLZ9zm5E2jc130_provenance.
- NP55987.RAlJO9SpFHWyfgV4jZ5XM0cx_GFCzzBwpzakbEKlUYEaw130_assertion description "[Significantly increased risk of pneumonitis was observed for patients with genetic variation in the proinflammatory genes IL1A, IL8, TNF, TNFRSF1B, and MIF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55987.RAlJO9SpFHWyfgV4jZ5XM0cx_GFCzzBwpzakbEKlUYEaw130_provenance.
- NP55988.RAmt53aG1Vk5m8Yvb7nt7jplamw64xOBPA8MOV7uWRL5M130_assertion description "[These results provide support for genetic predisposition to QOL and symptom burden and may aid in identification of lung cancer survivors at high risk for symptom management and QOL difficulties.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55988.RAmt53aG1Vk5m8Yvb7nt7jplamw64xOBPA8MOV7uWRL5M130_provenance.
- NP55991.RAidZroTxzvKReWGLGjsyMqctt-csfAG_N5fuyNmuAo2s130_assertion description "[Cytokine and cytokine receptor single-nucleotide polymorphisms predict risk for non-small cell lung cancer among women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55991.RAidZroTxzvKReWGLGjsyMqctt-csfAG_N5fuyNmuAo2s130_provenance.