Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP52395.RAlTroEcCj3_raZN0y5WzwrUbhflg38TwLYXdTk22lDvE130_assertion description "[ We can speculate that susceptibility to the development of chronic periodontitis could be influenced by the 1704G/T polymorphism of the RAGE gene, independently of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52395.RAlTroEcCj3_raZN0y5WzwrUbhflg38TwLYXdTk22lDvE130_provenance.
- NP52408.RAge2J2NvkiNrnFKn8UzwIT8TsgfJDk_H0lBqxuWAVCts130_assertion description "[Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52408.RAge2J2NvkiNrnFKn8UzwIT8TsgfJDk_H0lBqxuWAVCts130_provenance.
- NP52414.RAmEqw0LzEg6hCGAVMSQQNbuO7l4CwMhJBy_6ZRRdaz9k130_assertion description "[Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52414.RAmEqw0LzEg6hCGAVMSQQNbuO7l4CwMhJBy_6ZRRdaz9k130_provenance.
- NP52418.RAhQRgtA6RgXfQOLSqPU00G1F7xxzJaNlf0gdpTFA6g7I130_assertion description "[Thus, 135G-->C may modify the risk of breast cancer in BRCA2 mutation carriers by altering the expression of RAD51.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52418.RAhQRgtA6RgXfQOLSqPU00G1F7xxzJaNlf0gdpTFA6g7I130_provenance.
- NP52421.RAteVOmMqQpcqGU0Pd5UFaO6DlXza6LxWmN04uktdzo4A130_assertion description "[RAD51 G135C polymorphism is associated with breast cancer susceptibility: a meta-analysis involving 22,399 subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52421.RAteVOmMqQpcqGU0Pd5UFaO6DlXza6LxWmN04uktdzo4A130_provenance.
- NP52427.RAqwbg68Pz8QS6yCpV93gjb2Ux5QIChsirchYBFdendZM130_assertion description "[In summary, our results suggest that genetic variants in genes involved in the NER pathway may play a role in lung cancer susceptibility in Xuan Wei. However, due to the small sample size, additional studies are needed to evaluate these associations within Xuan Wei and in other populations with substantial environmental exposure to PAHs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52427.RAqwbg68Pz8QS6yCpV93gjb2Ux5QIChsirchYBFdendZM130_provenance.
- NP52433.RApu9KIQplMrj7ll8F9QWwBv2FaagJs9RW1P0KV_9U76c130_assertion description "[Our data suggest that the PYY-Y2R pathway may influence body weight through a sex-specific mechanism, but this finding requires confirmation in other populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52433.RApu9KIQplMrj7ll8F9QWwBv2FaagJs9RW1P0KV_9U76c130_provenance.
- NP52434.RAp2GVDxCUOeu-dC8nIWT_e8KNoCm8eOj5XoeO0I8Fu5Q130_assertion description "[Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52434.RAp2GVDxCUOeu-dC8nIWT_e8KNoCm8eOj5XoeO0I8Fu5Q130_provenance.
- NP52439.RAsJRAkDZV4PoyvLApbrqtqxLjT539B6fg9_fhlo1i6ps130_assertion description "[In Caucasians, LEP SNPs also tended to be associated with weight (p = 0.0471), and PYY rs11684664 was associated with obesity-related phenotypes in women only (p = 0.010-0.026).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52439.RAsJRAkDZV4PoyvLApbrqtqxLjT539B6fg9_fhlo1i6ps130_provenance.
- NP52448.RAl_7HeOCMq8I3p4cpgWYcWtEbU6NM1TQ5R0gUq0wveds130_assertion description "[The 77C->G mutation in the human CD45 (PTPRC) gene leads to increased intensity of TCR signaling in T cell lines from healthy individuals and patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52448.RAl_7HeOCMq8I3p4cpgWYcWtEbU6NM1TQ5R0gUq0wveds130_provenance.
- NP52451.RAhQZ0AaQ7ozlp9w275HL_iP52-HZLkhKJ7T1YcWmsXsA130_assertion description "[A point mutation in PTPRC is associated with the development of multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52451.RAhQZ0AaQ7ozlp9w275HL_iP52-HZLkhKJ7T1YcWmsXsA130_provenance.
- NP52453.RArpUVnnBhQQB5020LDKWuMYbpl3ijnYsuggQPH4zJh-E130_assertion description "[ C77G is present in the Spanish population. Further studies to elucidate its clinical significance are needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52453.RArpUVnnBhQQB5020LDKWuMYbpl3ijnYsuggQPH4zJh-E130_provenance.
- NP52457.RAgZsJ_kmoJPPf6Hc8VpEwiMnL3D5aXskjzIMRYyQYSSw130_assertion description "[The observed data could not be explained by the role of a single variant but were compatible either with a joint effect of the three typed SNPs of PTPN22 on RA or with the role of two untyped variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52457.RAgZsJ_kmoJPPf6Hc8VpEwiMnL3D5aXskjzIMRYyQYSSw130_provenance.
- NP52464.RAhKMQS2r7cuMJuXbYAZQmmkVDNwgIbuGoSyxqlCrE1H0130_assertion description "[Here we report the association of RA susceptibility with the minor allele of a missense SNP in PTPN22 (discovery-study allelic P=6.6 x 10(-4); replication-study allelic P=5.6 x 10(-8)), which encodes a hematopoietic-specific protein tyrosine phosphatase also known as `Lyp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52464.RAhKMQS2r7cuMJuXbYAZQmmkVDNwgIbuGoSyxqlCrE1H0130_provenance.
- NP52476.RAlZuq7i09i5q7swQHvB0K2bOJL6fPdGAEwZRFL1po98s130_assertion description "[Association analysis of the PTPN22 gene in childhood-onset systemic lupus erythematosus in Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52476.RAlZuq7i09i5q7swQHvB0K2bOJL6fPdGAEwZRFL1po98s130_provenance.
- NP52479.RAuuA1Jh6AFmbXUFFvboi_5eJflTpNmSdAzQxxVZlLJHs130_assertion description "[The autoimmune disease risk allele of PTPN22 is associated with skewing of serum cytokine profiles toward higher IFNalpha activity and lower TNFalpha levels in vivo in patients with SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52479.RAuuA1Jh6AFmbXUFFvboi_5eJflTpNmSdAzQxxVZlLJHs130_provenance.
- NP52482.RAhSbjSTcfpSHOwox1GIMxZR0jBJhTgdsCFgRqTlsfPgU130_assertion description "[The autoimmune disease risk allele of PTPN22 is associated with skewing of serum cytokine profiles toward higher IFNalpha activity and lower TNFalpha levels in vivo in patients with SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52482.RAhSbjSTcfpSHOwox1GIMxZR0jBJhTgdsCFgRqTlsfPgU130_provenance.
- NP52484.RAl51EyOXWv76urvCzCVW5wZEkXwON9i2jeb7aeK3XWSQ130_assertion description "[ The role of the Apo-1/Fas gene promoter MvaI polymorphism in RA and SLE is unclear and further substantiation in larger patient samples is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52484.RAl51EyOXWv76urvCzCVW5wZEkXwON9i2jeb7aeK3XWSQ130_provenance.
- NP52485.RArkci5iKFwvAzU0i5YzBpKd8gk5QTblRWa-JdMqGS82I130_assertion description "[Investigation of the -1377 polymorphism on the Apo-1/Fas promoter in systemic lupus erythematosus patients using allele-specific amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52485.RArkci5iKFwvAzU0i5YzBpKd8gk5QTblRWa-JdMqGS82I130_provenance.
- NP52487.RArfyX4CXpDnDmTYfm0q4sYeqH7BDv8PVQYUEdAVuFmjE130_assertion description "[In 2001 a gene responsible for Noonan syndrome, PTPN11, encoding for the non-receptor protein tyrosine phosphatase SHP-2, was identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52487.RArfyX4CXpDnDmTYfm0q4sYeqH7BDv8PVQYUEdAVuFmjE130_provenance.
- NP52488.RAgKDGoL6ZfR0kiTZrQjAXMsAysHUvprcevDmMgMkXymI130_assertion description "[PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52488.RAgKDGoL6ZfR0kiTZrQjAXMsAysHUvprcevDmMgMkXymI130_provenance.
- NP52489.RAqJXyfgC2N4bqe9CHnZXljD4sTycxN9SlWV_1oMUys-g130_assertion description "[The phenotype of NS due to PTPN11 mutations is clinically unambiguous in the majority of patients and represents a highly penetrant trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52489.RAqJXyfgC2N4bqe9CHnZXljD4sTycxN9SlWV_1oMUys-g130_provenance.
- NP52490.RAnul162exreqTlQ00JFaCKlLVcifsM7-kDjcSsDjKPHQ130_assertion description "[The results suggest that PTPN11 mutations account for approximately 40% of Noonan syndrome patients, as has been reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52490.RAnul162exreqTlQ00JFaCKlLVcifsM7-kDjcSsDjKPHQ130_provenance.
- NP52499.RApk4Gsn8rbA3cUd3ALK_mUppHFVb-mW3YrafkPP-_W54130_assertion description "[Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52499.RApk4Gsn8rbA3cUd3ALK_mUppHFVb-mW3YrafkPP-_W54130_provenance.
- NP52502.RAnGipXagqrky3H3XQzJBTKttpr77g3I8bVmu0OxSgCmI130_assertion description "[The alanine variant of the Pro12Ala polymorphism of PPARgamma might be associated with decreased risk of DR in T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52502.RAnGipXagqrky3H3XQzJBTKttpr77g3I8bVmu0OxSgCmI130_provenance.
- NP52503.RAm-FODnBfJBcNVJSPXjZlUi8w66H7g92E5EJ-_PE-JiY130_assertion description "[We screened 2.0 kb of PTPN1 promoter in 174 T2D patients and 412 controls using PCR and denaturing HPLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52503.RAm-FODnBfJBcNVJSPXjZlUi8w66H7g92E5EJ-_PE-JiY130_provenance.
- NP52504.RAjkhjw8Ju2LJPKKEXu8lfICXBBq1P9GSeJwme471IVGk130_assertion description "[Our results support the hypothesis that the PTP 1B gene contributes to the polygenic basis of obesity. PTP 1B SNPs may interact with environmental factors to induce more severe phenotypes, e.g. atherogenic dyslipidaemia, in morbidly obese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52504.RAjkhjw8Ju2LJPKKEXu8lfICXBBq1P9GSeJwme471IVGk130_provenance.
- NP52511.RAngRgoXD4zzpaHIxrB6KPOXuemO08yKJX75hj0_WZaeM130_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." NP52511.RAngRgoXD4zzpaHIxrB6KPOXuemO08yKJX75hj0_WZaeM130_provenance.
- NP52512.RAjhIstTnrXfyjAs5MpnYoAy1G7fXIGIO4v8G-Jwg4WWs130_assertion description "[Association between parathyroid hormone (PTH)/PTH-related peptide receptor gene polymorphism and the extent of bone mass reduction in primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52512.RAjhIstTnrXfyjAs5MpnYoAy1G7fXIGIO4v8G-Jwg4WWs130_provenance.
- NP52513.RAi96uKz_TuR9OlvLiKQk6oFyXhLeXQNar0XBO6ua9l24130_assertion description "[Polymorphisms associated with asthma are inversely related to glioblastoma multiforme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52513.RAi96uKz_TuR9OlvLiKQk6oFyXhLeXQNar0XBO6ua9l24130_provenance.
- NP52514.RApN2Xxju69fFIWvAuXdhU2z5YSh-433eO7PtqqPhELoc130_assertion description "[The role of the COX-2 926G>C Single Nucleotide Polymorphism (SNP) in patients with NSCLC remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52514.RApN2Xxju69fFIWvAuXdhU2z5YSh-433eO7PtqqPhELoc130_provenance.
- NP52515.RAg7gWc5HNNArZOPwuSgOeJfGhj6mw1DkK9lTVL7Jtazk130_assertion description "[These results provide evidence that the A allele of Cox-2 intron 6 may be associated with the development of lung cancer and may be a useful marker for early detection and treatment of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52515.RAg7gWc5HNNArZOPwuSgOeJfGhj6mw1DkK9lTVL7Jtazk130_provenance.
- NP52520.RAreVJSFMnWJonbiB90VInLd-tr8pkXNM1VVAxYtpZxek130_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." NP52520.RAreVJSFMnWJonbiB90VInLd-tr8pkXNM1VVAxYtpZxek130_provenance.
- NP52524.RAkR61wjCYRYr952meokyNRlAH-zAwjrHjavhYskWEVHI130_assertion description "[The PTGS2 8473T>C polymorphism was found to be correlated with PFS and OS in patients with advanced colorectal cancer treated with XELOX chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52524.RAkR61wjCYRYr952meokyNRlAH-zAwjrHjavhYskWEVHI130_provenance.
- NP52525.RAlgW8tkX_zWzuhgquSZQSWaIK3hYgkJKGZ_WxxwyUagk130_assertion description "[The -765C allele of the cyclooxygenase-2 gene as a potential risk factor of colorectal cancer: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52525.RAlgW8tkX_zWzuhgquSZQSWaIK3hYgkJKGZ_WxxwyUagk130_provenance.
- NP52531.RAjuHq1kq60BbUZ75eXdnd-hChck6r5FztJGxAaKRgy-s130_assertion description "[A case-control study was conducted, and 8 single nucleotide polymorphisms (SNP), including FAS - 670G/A, FAS - 1377G/A, FASL -844T/C, COX-2 - 1290A/G, COX-2 - 1195G/A, STK15 Phe31Ile, MMP-2 - 1306C/T and MMP -2 -735C/T, were detected by polymerase chain reaction-based restriction fragment length polymorphism assay (PCR-RFLP) in 188 esophageal cancer cases and 324 normal controls of Mongolian.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52531.RAjuHq1kq60BbUZ75eXdnd-hChck6r5FztJGxAaKRgy-s130_provenance.
- NP52534.RAs6aemRLZ6uCm1yHDo_vnADC77IsVofG2DJWH98zYdMc130_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." NP52534.RAs6aemRLZ6uCm1yHDo_vnADC77IsVofG2DJWH98zYdMc130_provenance.
- NP52541.RAjjRrb0EQhjiQbJfihVi8x-DY5stIPrVot2FdzIoh0VM130_assertion description "[Toll-like receptor signaling pathway variants and prostate cancer mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52541.RAjjRrb0EQhjiQbJfihVi8x-DY5stIPrVot2FdzIoh0VM130_provenance.
- NP52544.RAr8b0n7gtG79L5RRzSxtCiouf52PZtSm9CJVjQnagePs130_assertion description "[Although COX-2 expression may be genetically determined, the relation between COX-2 polymorphisms and the risk of MI and stroke is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52544.RAr8b0n7gtG79L5RRzSxtCiouf52PZtSm9CJVjQnagePs130_provenance.
- NP52548.RAkqCVLxyCekZGsSTeN3spPmuxmc4XMdc9G0Ev9PuJMwg130_assertion description "[Cyclooxygenase-1 (COX-1) regulates the biosynthesis of prostaglandins, which are important mediators in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52548.RAkqCVLxyCekZGsSTeN3spPmuxmc4XMdc9G0Ev9PuJMwg130_provenance.
- NP52550.RAvut6x3iDDa989Y5fUcT2RACG62HZslTA1M4ti45aA5Y130_assertion description "[Splicing mutation of the prostacyclin synthase gene in a family associated with hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52550.RAvut6x3iDDa989Y5fUcT2RACG62HZslTA1M4ti45aA5Y130_provenance.
- NP52555.RAkNuH01F_scmnoUql_Il8E8jB3bBw35n7bo_cBt0iqw8130_assertion description "[ We conclude that the C1117A polymorphism in exon 8 is associated with risk for MI and may be a genetic marker of MI in Japanese persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52555.RAkNuH01F_scmnoUql_Il8E8jB3bBw35n7bo_cBt0iqw8130_provenance.
- NP52564.RAu-MO-HzKhkz_nTvTShhZijoB6vJsmPIt8Oyb3ZV36nU130_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." NP52564.RAu-MO-HzKhkz_nTvTShhZijoB6vJsmPIt8Oyb3ZV36nU130_provenance.
- NP52565.RArsgYu88k-JBa4eYis8l9RBfQnzZNHU6tdNoFFesJbrw130_assertion description "[Our functional and genetic findings identify PTGDR as an asthma-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52565.RArsgYu88k-JBa4eYis8l9RBfQnzZNHU6tdNoFFesJbrw130_provenance.
- NP52569.RAlagQk5jPkebr2CfrlqCYbfjzBZApJsPonZkmI9NXLzQ130_assertion description "[The results indicate that the evaluation of PTEN mutation and MIB-1 LI are useful to predict dissemination and prognosis of glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52569.RAlagQk5jPkebr2CfrlqCYbfjzBZApJsPonZkmI9NXLzQ130_provenance.
- NP52573.RAgxzLEWYycvOwS0q6iSDAmkJ7cTVJJ0dqrHmAG0JMmlE130_assertion description "[Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52573.RAgxzLEWYycvOwS0q6iSDAmkJ7cTVJJ0dqrHmAG0JMmlE130_provenance.
- NP52574.RAvLZHMVXdrktMKYIUCMQGR0ZmSJvz7XFJwvFwMoCYopQ130_assertion description "[These findings suggest that the change of C to G at position -9 of the PTEN gene is associated with the insulin resistance of type 2 diabetes due possibly to a potentiated hydrolysis of the PI3-kinase product.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52574.RAvLZHMVXdrktMKYIUCMQGR0ZmSJvz7XFJwvFwMoCYopQ130_provenance.
- NP52578.RAtzxvw_5Ej9tvgSMOf69fgj5QKHIHMWEWpeUZZANr9rM130_assertion description "[Loss of PTEN function in breast cancer can occur either by mutation or reduction of PTEN expression in almost half of sporadic breast tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52578.RAtzxvw_5Ej9tvgSMOf69fgj5QKHIHMWEWpeUZZANr9rM130_provenance.
- NP52582.RAhDk7Y8sYFu0uR4jVkjBrc_lZK-867dwjamzq-DxAO3o130_assertion description "[No phenotype-genotype relationships were found in the Japanese NBCCS patients, consistent with results of previous studies on NBCCS in African-American and Caucasian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52582.RAhDk7Y8sYFu0uR4jVkjBrc_lZK-867dwjamzq-DxAO3o130_provenance.
- NP52583.RAk6jqwOv8F7s4ro1adqskgMBFYaABL3n73tbbAA2Oimo130_assertion description "[These data, showing for the first time that PTCH polymorphism mediates susceptibility, are compatible with reports showing that PTCH haploinsufficiency influences development of BCC precursor lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52583.RAk6jqwOv8F7s4ro1adqskgMBFYaABL3n73tbbAA2Oimo130_provenance.
- NP52596.RAjk0_4SRvGQPwu46y_DhjFdm_atG2qdBpPMQHKK2jGnQ130_assertion description "[To determine if a polymorphism in the immunoproteasome subunit LMP7 was associated with juvenile rheumatoid arthritis (JRA) and had functional significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52596.RAjk0_4SRvGQPwu46y_DhjFdm_atG2qdBpPMQHKK2jGnQ130_provenance.
- NP52600.RAqPoQtyAU9EZScdgLiKTRW6Ex8cy9aCcVJDLqCLbEkYA130_assertion description "[Of the seven polymorphisms, three of which (LMP7 codons 145, TAP1 codons 637, and TAP2 codons 651) were observed to have statistically significant association with HBV infection (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52600.RAqPoQtyAU9EZScdgLiKTRW6Ex8cy9aCcVJDLqCLbEkYA130_provenance.
- NP52621.RAsWpUIY8aViFhyjoEHLk7NmhgI6a4eMk9K3t0HAe_RZE130_assertion description "[We sought to establish an association between sporadic Alzheimer's disease (AD) and presenilin 1 (PSEN1) gene polymorphisms in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52621.RAsWpUIY8aViFhyjoEHLk7NmhgI6a4eMk9K3t0HAe_RZE130_provenance.
- NP52622.RAvSICXMuzh7-xTWCm_5MQ785kW7z7Ml1RGHpcUJJQse0130_assertion description "[We therefore hypothesized that linkage disequilibrium between the intronic PSEN1 polymorphism and the functional promoter polymorphism might explain the conflicting reports in LOAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52622.RAvSICXMuzh7-xTWCm_5MQ785kW7z7Ml1RGHpcUJJQse0130_provenance.
- NP52627.RAjM32Ny4t9d-lCSJi2esHFs1aW0Pz3ZK_e48ihWcYh30130_assertion description "[A genetic association between a polymorphism in intron 8 of the PS-1 gene and AD has been described in some series, and an increased risk of AD has been reported in mothers of DS probands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52627.RAjM32Ny4t9d-lCSJi2esHFs1aW0Pz3ZK_e48ihWcYh30130_provenance.
- NP52635.RAnfLm5BncjRWl3-zYe0OJAFaZD5Zme3qdUf3Qaz7MKGs130_assertion description "[In conclusion, our data suggest that CP may be inherited in a dominant, recessive or multigenetic manner as a result of mutations in the above-mentioned or as yet unidentified genes. This challenges the concept of idiopathic CP as a nongenetic disorder and the differentiation between hereditary and idiopathic CP. Therefore, we propose to classify CP as either 'primary CP' (with or without a family history) or 'secondary CP' caused by toxic, metabolic or other factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52635.RAnfLm5BncjRWl3-zYe0OJAFaZD5Zme3qdUf3Qaz7MKGs130_provenance.
- NP52652.RAsCLs_TmLk4_bivsqLrTdZ02u9bOhUQT9kqcDh4_XlD0130_assertion description "[The A allele of an intron F polymorphism of the PZ gene appears to be a novel protective genetic marker for the risk of cerebral ischemia in young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52652.RAsCLs_TmLk4_bivsqLrTdZ02u9bOhUQT9kqcDh4_XlD0130_provenance.
- NP52653.RAkV0tF5O-A3kVUivjGh5wdtrSVk00SYFQQ3VAGAukiVA130_assertion description "[Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52653.RAkV0tF5O-A3kVUivjGh5wdtrSVk00SYFQQ3VAGAukiVA130_provenance.
- NP52655.RAjth_gZFtRySanoSosDzS19uormbDWgvneciL-fQLixo130_assertion description "[A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52655.RAjth_gZFtRySanoSosDzS19uormbDWgvneciL-fQLixo130_provenance.
- NP52659.RArj2CMxsgpH52rkhPLIyevoLYbfce6QBnoz-eX2MX8og130_assertion description "[PRODH, encoding proline oxidase (POX), has been associated with schizophrenia through linkage, association, and the 22q11 deletion syndrome (Velo-Cardio-Facial syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52659.RArj2CMxsgpH52rkhPLIyevoLYbfce6QBnoz-eX2MX8og130_provenance.
- NP52661.RAgg5vD0l7hEkM-cQ2FMjcsF41O12SPoQ1qh8ecXpEZ38130_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." NP52661.RAgg5vD0l7hEkM-cQ2FMjcsF41O12SPoQ1qh8ecXpEZ38130_provenance.
- NP52665.RAj9b07l5a5Uq62R_Sx4o27W92MfjAglkvheSdJJN7ia4130_assertion description "[Thus, the A3 haplotype, which is associated with elevated plasma sEPCR levels, is a candidate risk factor for venous thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52665.RAj9b07l5a5Uq62R_Sx4o27W92MfjAglkvheSdJJN7ia4130_provenance.
- NP52667.RAkU_Xp08itBXxo9zpgkHgP_YIVPjY3Go1n_GtR1eOlyA130_assertion description "[Influence of the 4600A/G and 4678G/C polymorphisms in the endothelial protein C receptor (EPCR) gene on the risk of venous thromboembolism in carriers of factor V Leiden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52667.RAkU_Xp08itBXxo9zpgkHgP_YIVPjY3Go1n_GtR1eOlyA130_provenance.
- NP52681.RAks0ME3AtoBGHJ866umn88WWP99oilb6VhTNkIOJFkRw130_assertion description "[Since homozygosity MM at codon 129 of the prion protein gene is a recognised risk factor in all forms of Creutzfeldt-Jakob disease (CJD), we studied the distribution of codon 129 polymorphism in patients in France and in the UK with CJD transmitted iatrogenically by human growth hormone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52681.RAks0ME3AtoBGHJ866umn88WWP99oilb6VhTNkIOJFkRw130_provenance.
- NP52686.RAmdkWPORT4fzAq0A1uZDxiE7uvzc8qEJxrH73E6GRwA0130_assertion description "[Earlier onset of Alzheimer's disease: risk polymorphisms within PRNP, PRND, CYP46, and APOE genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52686.RAmdkWPORT4fzAq0A1uZDxiE7uvzc8qEJxrH73E6GRwA0130_provenance.
- NP52687.RAtrS49CEfcEO5S-26F7EDDyLkzL_xxf59JlVYZ0cneJc130_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." NP52687.RAtrS49CEfcEO5S-26F7EDDyLkzL_xxf59JlVYZ0cneJc130_provenance.
- NP52688.RAv0OdK6vEZyAe5Ss040re60wrkU6a2sfXO3ko6h4hnMI130_assertion description "[Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52688.RAv0OdK6vEZyAe5Ss040re60wrkU6a2sfXO3ko6h4hnMI130_provenance.
- NP52692.RAqVmjkMeY232HjYP1eBRYZVcMVDStIvudVM7X-lE-3Q4130_assertion description "[PRNP M129V homozygosity in multiple system atrophy vs. Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52692.RAqVmjkMeY232HjYP1eBRYZVcMVDStIvudVM7X-lE-3Q4130_provenance.
- NP52694.RAl0X_nKsg2OVGBqY-Y60PyJb1gg4wTrf1QIxA36aq8lY130_assertion description "[No case of variant CJD was registered. The study confirms in our population the consistent pattern reported worldwide on human prion diseases. Atypical features were seen more frequently in sporadic 129 V/V CJD and fCJD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52694.RAl0X_nKsg2OVGBqY-Y60PyJb1gg4wTrf1QIxA36aq8lY130_provenance.
- NP52701.RAnkzE50K5g_DgBPpRQJCyrudIODdvgrHdhrjZis9UMho130_assertion description "[These findings are relevant to the current outbreak of variant Creutzfeldt-Jakob disease (vCJD) in the United Kingdom, because all vCJD patients tested thus far have been M/M carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52701.RAnkzE50K5g_DgBPpRQJCyrudIODdvgrHdhrjZis9UMho130_provenance.
- NP52713.RAsqgwh4AyiNJAjymUtUfp5QSwcIa89Ob_NU4AJPXRmdM130_assertion description "[Statistical analysis revealed a significant difference in the distribution of the Prnd genotype at codon 174 between sporadic CJD patients and healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52713.RAsqgwh4AyiNJAjymUtUfp5QSwcIa89Ob_NU4AJPXRmdM130_provenance.
- NP52717.RAqVNYnHCxBsozewt3Ab9LfqkBzT7Ona9jS2GGf6X2kBo130_assertion description "[In fact: (1) a prolactin secretion dysfunction has been described in several autoimmune diseases including SLE and MS and their animal models; (2) both PRL and PRLR are structurally related to members of the cytokine/hematopoietin family and have a role in the regulation of the immune response; and (3) both PRL and PRLR genes map in genomic regions that showed linkage with autoimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52717.RAqVNYnHCxBsozewt3Ab9LfqkBzT7Ona9jS2GGf6X2kBo130_provenance.
- NP52719.RAlyoVYRmrg1SuNHaDEz8ilMkYqPvGuVo1Pwiq1SCGgMU130_assertion description "[Based on comprehensive NHEJ gene profiles, this study provides new insights to suggest the role of the NHEJ pathway in breast cancer development and supports the possibility that breast cancer is initiated by estrogen exposure, which causes DNA DSBs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52719.RAlyoVYRmrg1SuNHaDEz8ilMkYqPvGuVo1Pwiq1SCGgMU130_provenance.
- NP52721.RAj5V1MQR0r9Ss8zdMHXiJfdouGmt51ki7YUT7eV35r64130_assertion description "[Comprehensive screen of genetic variation in DNA repair pathway genes and postmenopausal breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52721.RAj5V1MQR0r9Ss8zdMHXiJfdouGmt51ki7YUT7eV35r64130_provenance.
- NP52724.RAmIrQvCSHfv1xm_6To4cy3YJm0-60CFBwsDsYfYbOjyM130_assertion description "[ The two SNP may be associated with type 2 diabetes in Han people of China, which makes base for further study of the relation between the genes they located with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52724.RAmIrQvCSHfv1xm_6To4cy3YJm0-60CFBwsDsYfYbOjyM130_provenance.
- NP52726.RAoLxd5StvOHfA-DtD1FUfNquGELzSbyX5szmTUidlxRg130_assertion description "[Protein kinase C/zeta (PRKCZ) gene is associated with type 2 diabetes in Han population of North China and analysis of its haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52726.RAoLxd5StvOHfA-DtD1FUfNquGELzSbyX5szmTUidlxRg130_provenance.
- NP52736.RAjuhLKc5s7O7Cm6dNf58GII_Jv56afc4y4p2OdIUw87M130_assertion description "[The positive association suggests that the PICK1 gene may play a role in the pathogenesis of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52736.RAjuhLKc5s7O7Cm6dNf58GII_Jv56afc4y4p2OdIUw87M130_provenance.
- NP52738.RArOCXKd9U_Q_JBbcDKW1OvRlpe3BW8FyBsrQ4_Wm6qn4130_assertion description "[Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52738.RArOCXKd9U_Q_JBbcDKW1OvRlpe3BW8FyBsrQ4_Wm6qn4130_provenance.
- NP52750.RAlmPsmE9dMJUlrd6DmOhWS3ZdK-_49ZOQkvD5n0zK2Cg130_assertion description "[To determine whether the muscle-specific glycogen-targeting regulatory subunit of the glucogen bound protein phosphatase 1 (PPP1R3) gene 5 bp deletion/insertion(D/I) within 3'-untranslated region ( 3'-UTR) polymorphism is associated with type 2 diabetes in Chinese Han population in Hefei region of Anhui province.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52750.RAlmPsmE9dMJUlrd6DmOhWS3ZdK-_49ZOQkvD5n0zK2Cg130_provenance.
- NP52751.RAgJjYYtWwKUt9rZPifk087aQPexRlXUPnH4I3HjFhHPk130_assertion description "[PPP1R3 gene Asp905Tyr polymorphism did not seem to play a critical role in the development of type 2 diabetes mellitus in Han population of Chinese in Anhui province but interaction between the Asp905 and BMI cause the increase of risk of type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52751.RAgJjYYtWwKUt9rZPifk087aQPexRlXUPnH4I3HjFhHPk130_provenance.
- NP52753.RAkGbhCMZKIqighbgbE0KGD_r6s5vErI1lxsQEozPkFV0130_assertion description "[To detect the relationship between the polymorphism of the glycogen-targeting regulatory subunit of the skeletal muscle glycogen-associated protein phosphatase 1 (PPP1R3) gene and type 2 diabetes by case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52753.RAkGbhCMZKIqighbgbE0KGD_r6s5vErI1lxsQEozPkFV0130_provenance.
- NP52754.RAlmq_zzCiyYgUql9LwlGYrW1Ha1qWqE6fl4JxXidbrqc130_assertion description "[The 3'-untranslated region polymorphism of the gene for skeletal muscle-specific glycogen-targeting subunit of protein phosphatase 1 in the type 2 diabetic Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52754.RAlmq_zzCiyYgUql9LwlGYrW1Ha1qWqE6fl4JxXidbrqc130_provenance.
- NP52758.RAieAXQ5zJN2Eno_eTWTpiJbJeFk74ggzLBx9DMh4NqXQ130_assertion description "[The peroxisome proliferator-activated receptor-gamma ( PPARG) Pro12Ala and the PPARG co-activator-1alpha ( PPARGC1A) Gly482Ser polymorphisms (SNPs) have been associated with type 2 diabetes mellitus (T2DM) risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52758.RAieAXQ5zJN2Eno_eTWTpiJbJeFk74ggzLBx9DMh4NqXQ130_provenance.
- NP52759.RApLH1CxiFaRl0HMG7NJc3fMjUKrfRMsSEYYSAzJIIozA130_assertion description "[To investigate the association between single nucleotide polymorphisms (SNPs) rs2970847(Thr394Thr) and rs8192678(Gly482Ser) of peroxisome proliferators activated receptor gamma coactivator-1(PPARGC1A)gene and type 2 diabetes in Chinese Han population in Hubei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52759.RApLH1CxiFaRl0HMG7NJc3fMjUKrfRMsSEYYSAzJIIozA130_provenance.
- NP52763.RAppiqVwiX8q0oCvwhOck9hDHFMWEkQswi4lpOno5K_VE130_assertion description "[The A allele of the Thr394Thr (G-->A) polymorphism of the PPARGC1A gene was associated with insulin resistance, and may be related to central obesity and decreased HDL-C levels in Chinese population. The relationship between this polymorphism and T2DM needs further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52763.RAppiqVwiX8q0oCvwhOck9hDHFMWEkQswi4lpOno5K_VE130_provenance.
- NP52773.RAnSL3xtyLtoOd3Y12NAMUU4pR5DnlKDfkP5DWnGOw8ns130_assertion description "[The objective of the study was to o investigate the relationship of the Gly482Ser (G482S) polymorphism in the peroxisome proliferator-activated receptor gamma coactivator-1alpha (PPARGC1A) gene and type 2 diabetes mellitus (T2DM), obesity, and oxidative status in Chinese adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52773.RAnSL3xtyLtoOd3Y12NAMUU4pR5DnlKDfkP5DWnGOw8ns130_provenance.
- NP52775.RAuOhWl3Nc1XwVQfPrr9tZDHyeKmDyhzZYo6Idtc9BuVo130_assertion description "[In conclusion, the Ser allele of PGC-1alpha Gly482Ser confers a significantly reduced risk of hypertension in whites. Further studies are needed to elucidate the differential role of this polymorphism in men and women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52775.RAuOhWl3Nc1XwVQfPrr9tZDHyeKmDyhzZYo6Idtc9BuVo130_provenance.
- NP52776.RAoOmFIRsFHg2_7PM01p_mKHTe_a9UikAJomw4_4qxB_g130_assertion description "[These results suggest, but do not prove, that PPARGC1 participates in blood pressure control, and sequence substitutions at its gene locus confer an increased risk of hypertension to a substantial proportion of men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52776.RAoOmFIRsFHg2_7PM01p_mKHTe_a9UikAJomw4_4qxB_g130_provenance.
- NP52777.RApPpy0PdemFgSKTM4BkQdmYs0ywo_Hip6j8Bc5RSvSu8130_assertion description "[The Gly482Ser genotype at the PPARGC1A gene and elevated blood pressure: a meta-analysis involving 13,949 individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52777.RApPpy0PdemFgSKTM4BkQdmYs0ywo_Hip6j8Bc5RSvSu8130_provenance.
- NP52787.RAk75e2bgQXfArnrxutqeolrlyO5uWeQ4m5Hhg-2I0jUE130_assertion description "[ Both analyzed polymorphisms were associated in a synergistic manner with hypertension. This effect manifested only in those subjects with normal homocysteine plasma values. Our findings suggest complex genotype-environmental interactions on hypertensive risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52787.RAk75e2bgQXfArnrxutqeolrlyO5uWeQ4m5Hhg-2I0jUE130_provenance.
- NP52788.RAqMfvbPaRDyeFZ_sNLQjmawqTRnla1n8kK5nki0aV4NY130_assertion description "[Our results highlight the potential of microarray-based technology for SNP genotyping in pharmacogenetics.(1)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52788.RAqMfvbPaRDyeFZ_sNLQjmawqTRnla1n8kK5nki0aV4NY130_provenance.
- NP52800.RAjblDlsDzddd6ZXQ_-L573HF4SEnE8XSK4fOFVWj7o-s130_assertion description "[Effects of a PPARG gene variant on obesity characteristics in Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52800.RAjblDlsDzddd6ZXQ_-L573HF4SEnE8XSK4fOFVWj7o-s130_provenance.
- NP52810.RAtnhVaSjl7THo5XT1gUvSg-kHKnCQt2JmMNzoJyfCcV4130_assertion description "[This is the first study implicating polymorphisms in inflammatory genes to the risk of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52810.RAtnhVaSjl7THo5XT1gUvSg-kHKnCQt2JmMNzoJyfCcV4130_provenance.
- NP52813.RAhJZvgsKL8duhgLjfn8Djnswr_y4rwT7dRntu3li8NMQ130_assertion description "[Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52813.RAhJZvgsKL8duhgLjfn8Djnswr_y4rwT7dRntu3li8NMQ130_provenance.
- NP52815.RAox83nWgLmeSkU3KDsRjo_0S_VLxAWHm0O1DqdqLLE8o130_assertion description "[Genetic variants in peroxisome proliferator-activated receptor-gamma gene are associated with risk of lung cancer in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52815.RAox83nWgLmeSkU3KDsRjo_0S_VLxAWHm0O1DqdqLLE8o130_provenance.
- NP52821.RAm4Hkj7oc-J8dfMo_hUwktC37CW80AbVP44N7znWFDPs130_assertion description "[Together, these results showed that PPARG Pro12Ala and PPARGC1A Gly482Ser variants are associated, alone and in interaction, with insulin and glucose homeostasis and suggest that gene-gene interactions should be taken into account in candidate gene studies of T2DM to identify subjects with markedly different risks of developing the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52821.RAm4Hkj7oc-J8dfMo_hUwktC37CW80AbVP44N7znWFDPs130_provenance.
- NP52825.RAkMA1QhoqjPNBEZa8y3usiDCTb0rJupcsLji6PWAXVII130_assertion description "[Despite its association with lower BMI among T2DM patients, the PPARgamma gene does not appear to markedly influence Type 2 diabetes among Tunisian subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52825.RAkMA1QhoqjPNBEZa8y3usiDCTb0rJupcsLji6PWAXVII130_provenance.
- NP52826.RAm8mEyLIA5pgY-XADmjsR5y9UuS2CmhiODtci2p9ieyE130_assertion description "[1) The TNFalpha concentration in serum and the TNFalpha gene expression in monocytes do not refer to the Pro12ala polymorphism of PPARgamma in patients with type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52826.RAm8mEyLIA5pgY-XADmjsR5y9UuS2CmhiODtci2p9ieyE130_provenance.
- NP52827.RAhF-v1EuyMYFtZZe3PVRtbmVNsePlINZwfrebBHMXu-E130_assertion description "[SNPs in PPARG associate with type 2 diabetes and interact with physical activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52827.RAhF-v1EuyMYFtZZe3PVRtbmVNsePlINZwfrebBHMXu-E130_provenance.
- NP52830.RAp_v19BK6U54v9f1a6nIl9Pjwv2j6lrl1zzlVn6j_Hko130_assertion description "[Our data do not support a major role for the Pro12Ala variant of the PPARG gene in MetS and its individual components.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52830.RAp_v19BK6U54v9f1a6nIl9Pjwv2j6lrl1zzlVn6j_Hko130_provenance.