Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP85571.RAmZdYpTm0T1nAgVjEVAV-iEhBiYDFs03Kp52hsF1UXgo130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85571.RAmZdYpTm0T1nAgVjEVAV-iEhBiYDFs03Kp52hsF1UXgo130_provenance.
- NP85579.RAoEDbN-KiG54xAeXOrjwtR2Nes7Iy1tWbzCTcHq8VmIU130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85579.RAoEDbN-KiG54xAeXOrjwtR2Nes7Iy1tWbzCTcHq8VmIU130_provenance.
- NP85588.RAmHWYNhXzwsdynoVkhg1E0r7UFs7Lcnx0SotEHJlgA7o130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85588.RAmHWYNhXzwsdynoVkhg1E0r7UFs7Lcnx0SotEHJlgA7o130_provenance.
- NP85595.RAlHM4i10k8zfUafsD_EypDACz8ET7kBC6oKidDSrP_cs130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85595.RAlHM4i10k8zfUafsD_EypDACz8ET7kBC6oKidDSrP_cs130_provenance.
- NP85609.RAkgjI2_4prrgAczoHpdLXsW-H2hCCAKoRL-9Mo8Xlk74130_assertion description "[We have confirmed 7 loci associated with blood pressure and/or hypertension in the Japanese. These loci can guide fine-mapping efforts to pinpoint causal variants and causal genes with the integration of multiethnic results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85609.RAkgjI2_4prrgAczoHpdLXsW-H2hCCAKoRL-9Mo8Xlk74130_provenance.
- NP85622.RAuXbNiStJYqDhNl7BDUlnRSiCRJ5A8VhEJIiDjcAw9Qs130_assertion description "[All neurologic diseases, including MCI, had increased mortality versus controls. A lower MMSE score and APOE4 presence predicted higher mortality for some patient groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85622.RAuXbNiStJYqDhNl7BDUlnRSiCRJ5A8VhEJIiDjcAw9Qs130_provenance.
- NP85624.RAqftxkDo5MeXL7pAZUxHB7a-p-TW4BWal0VTISQdjrqk130_assertion description "[Depression and APOE act independently to increase the risk for cognitive decline and may provide targets for prevention and early treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85624.RAqftxkDo5MeXL7pAZUxHB7a-p-TW4BWal0VTISQdjrqk130_provenance.
- NP85625.RAjjUmIg-zNEF7W6fX2fPWe6BeZs7IgFyDOdYEn9eJXQI130_assertion description "[ApoE polymorphisms and diarrheal outcomes in Brazilian shanty town children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85625.RAjjUmIg-zNEF7W6fX2fPWe6BeZs7IgFyDOdYEn9eJXQI130_provenance.
- NP85627.RAraOS6QLPJLu2uNSXwaHwrmQeXJbgr94yHA7p7cLNNtw130_assertion description "[Decreased neurotrophic support, as indicated by a reduced systemic availability of BDNF, may play role in the neurodegenerative processes that underlie the continuum from MCI to AD. The presence of Met-BDNF allele, particularly in association with APOE*E4, may predict a worse cognitive outcome in patients with MCI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85627.RAraOS6QLPJLu2uNSXwaHwrmQeXJbgr94yHA7p7cLNNtw130_provenance.
- NP85632.RAmx_9YCWwEG2EoeMZiTXovKU6bkJQOT-r31XVkNbUKdo130_assertion description "[Energy balance, the PI3K-AKT-mTOR pathway genes, and the risk of bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85632.RAmx_9YCWwEG2EoeMZiTXovKU6bkJQOT-r31XVkNbUKdo130_provenance.
- NP85634.RAtBII5gLJGeumHpoV8CUhnildHP6TQ-eU0UFUtznpPM0130_assertion description "[This candidate gene analysis identified the potential role of genes operating through intermediate disease pathways to influence sleep apnea phenotypes, providing a framework for focusing future replication studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85634.RAtBII5gLJGeumHpoV8CUhnildHP6TQ-eU0UFUtznpPM0130_provenance.
- NP85640.RAtAL_k57WEGMnm_45bfRz_OUEW39yNi_QB4OJD_iBnEg130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85640.RAtAL_k57WEGMnm_45bfRz_OUEW39yNi_QB4OJD_iBnEg130_provenance.
- NP85646.RAglic8l3nXM3MVxyyZA-hxpmJS0WlBBIfWHsb3jWv06s130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85646.RAglic8l3nXM3MVxyyZA-hxpmJS0WlBBIfWHsb3jWv06s130_provenance.
- NP85647.RAnPFv_jpjRDVoGA9UuSZ2yhXou6VXxnFC3JuiF2Fe6Hw130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85647.RAnPFv_jpjRDVoGA9UuSZ2yhXou6VXxnFC3JuiF2Fe6Hw130_provenance.
- NP85648.RAgF_EJUDdk7gAuTy9AsocRN_QEiQTiK84UlRMMLEL4V8130_assertion description "[Adding SNPs previously associated with fasting glucose, insulin, lipids or obesity to a genetic risk score for type 2 diabetes significantly increases the power to discriminate between people with and without clinically manifest type 2 diabetes compared with a model including only conventional type 2 diabetes loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85648.RAgF_EJUDdk7gAuTy9AsocRN_QEiQTiK84UlRMMLEL4V8130_provenance.
- NP85657.RAtOc0TE1SeeWAVCcAtVZpgmLBNYpA2isEpNr1JL7t_5g130_assertion description "[Despite the small sample size, this novel analysis method identified an sMRI component including brain areas previously reported to be abnormal in schizophrenia and an associated genetic component containing several putative schizophrenia risk genes. Thus, we identified multiple genes potentially underlying specific structural brain abnormalities in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85657.RAtOc0TE1SeeWAVCcAtVZpgmLBNYpA2isEpNr1JL7t_5g130_provenance.
- NP85658.RAmQdmxWwIGoxaxVTc-8XwvtqDWnlHEN8co1Jm3bRRvmk130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The developed amplification strategy allows for the pooling of multiple patients with non-overlapping phenotypes, enabling many patients to be analyzed simultaneously in a fast and cost-effective manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85658.RAmQdmxWwIGoxaxVTc-8XwvtqDWnlHEN8co1Jm3bRRvmk130_provenance.
- NP85660.RAljTradDYq2aI6Rm3w5H968Wzdj3sd-C9Vqehi2oXYa8130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The developed amplification strategy allows for the pooling of multiple patients with non-overlapping phenotypes, enabling many patients to be analyzed simultaneously in a fast and cost-effective manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85660.RAljTradDYq2aI6Rm3w5H968Wzdj3sd-C9Vqehi2oXYa8130_provenance.
- NP85666.RAgAztJ7ugrpFcBgiHHtwq-vSZXajU4YmqZ2srye6fOsg130_assertion description "[Meta-analyses, which included 1655 T2D cases and 2911 control subjects, showed no association between any of the INSIG1 SNPs and T2D (P > 0.08).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85666.RAgAztJ7ugrpFcBgiHHtwq-vSZXajU4YmqZ2srye6fOsg130_provenance.
- NP85667.RArngi94P7-q-N_RBL4d1cx26hftE9u_ainYe2l66mS9c130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The developed amplification strategy allows for the pooling of multiple patients with non-overlapping phenotypes, enabling many patients to be analyzed simultaneously in a fast and cost-effective manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85667.RArngi94P7-q-N_RBL4d1cx26hftE9u_ainYe2l66mS9c130_provenance.
- NP85675.RAkQp8peMHdnY52hfOc-DEGA96UrjSAEjKj1qd7S1Z-nc130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85675.RAkQp8peMHdnY52hfOc-DEGA96UrjSAEjKj1qd7S1Z-nc130_provenance.
- NP85676.RAnRxguHfLJYQEGGT8ERirhDzVLYIeXWxwXvFPYQezlKY130_assertion description "[Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85676.RAnRxguHfLJYQEGGT8ERirhDzVLYIeXWxwXvFPYQezlKY130_provenance.
- NP85686.RAsBXvV2Q2gcSXvABV-goJ-dMa1U3N15-khU-1TFvRgdA130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85686.RAsBXvV2Q2gcSXvABV-goJ-dMa1U3N15-khU-1TFvRgdA130_provenance.
- NP85695.RApopRIvbhPG5dkr29Egao5EhUqei1qbKTLp_aYZBNrgo130_assertion description "[Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85695.RApopRIvbhPG5dkr29Egao5EhUqei1qbKTLp_aYZBNrgo130_provenance.
- NP85697.RAg4M4dfl2DzqRAO_jAb8VDPf_AKgk7n2LXTZzuUU4jOo130_assertion description "[Association of haplotypes in the CXCR2 gene with periodontitis in a Brazilian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85697.RAg4M4dfl2DzqRAO_jAb8VDPf_AKgk7n2LXTZzuUU4jOo130_provenance.
- NP85706.RApUPfhw5CvQdJ4R9UThtKFFC7OjxfK8HT75NI4n60ulc130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85706.RApUPfhw5CvQdJ4R9UThtKFFC7OjxfK8HT75NI4n60ulc130_provenance.
- NP85709.RAprrRCfR8CHWJiIeVfbfh9qip0o2RoLQh6R8oHjuiCNA130_assertion description "[Interleukin-8 -251 A/T gene polymorphism and gastric cancer susceptibility: a meta-analysis of epidemiological studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85709.RAprrRCfR8CHWJiIeVfbfh9qip0o2RoLQh6R8oHjuiCNA130_provenance.
- NP85713.RAhi5Z0LGHp7vERC2xqOUknQXfLXN5ngX-Ro1HuOwnmng130_assertion description "[Although none of the investigated SNPs in the IL8 gene was individually associated with periodontitis, some haplotypes showed significant association with susceptibility to, or protection against, chronic periodontitis in a Brazilian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85713.RAhi5Z0LGHp7vERC2xqOUknQXfLXN5ngX-Ro1HuOwnmng130_provenance.
- NP85718.RAoZX4N_t8T6kplxunZ7hMbUUDDD5i-y8BKOgJJ09Mql4130_assertion description "[Cytokine gene polymorphisms and risk for upper respiratory symptoms in highly-trained athletes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85718.RAoZX4N_t8T6kplxunZ7hMbUUDDD5i-y8BKOgJJ09Mql4130_provenance.
- NP85720.RAvy_J_boG4ZFwcpnPvRhSaVFpHM2PvFqt0sro0fe_cQk130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85720.RAvy_J_boG4ZFwcpnPvRhSaVFpHM2PvFqt0sro0fe_cQk130_provenance.
- NP85721.RAmeH7NagTxLZtC42ysdAmp_zsxZWYBR3Zb9vZgQzZB-8130_assertion description "[This study presents one of the first illustrations of successfully analyzing GWA data with a machine learning algorithm. It is shown that RF is computationally feasible for GWA data and the results obtained make biologic sense based on previous studies. More importantly, new genes were identified as potentially being associated with MS, suggesting new avenues of investigation for this complex disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85721.RAmeH7NagTxLZtC42ysdAmp_zsxZWYBR3Zb9vZgQzZB-8130_provenance.
- NP85723.RAk8eWhlx-z-KvLEMTxnd6i3YPSPzAq0K7QQCK87RwTRE130_assertion description "[Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility `hot-spot`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85723.RAk8eWhlx-z-KvLEMTxnd6i3YPSPzAq0K7QQCK87RwTRE130_provenance.
- NP85725.RAh1Y4NZyeTYr3gPdhMFdiOmj0zVXR_TuseuiMu0Z4uqI130_assertion description "[Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85725.RAh1Y4NZyeTYr3gPdhMFdiOmj0zVXR_TuseuiMu0Z4uqI130_provenance.
- NP85734.RAiWB0tl3kz0EB0W-ALFMkp6wqbZUPv-FtS_8DyOgAxs0130_assertion description "[Interestingly, the frequency of ICAM-1 EE homozygotes who concomitantly carried the IL-6 -634G allele was significantly higher in patients with endometriosis (chi(2) = 6.458, P = 0.0396, d.f.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85734.RAiWB0tl3kz0EB0W-ALFMkp6wqbZUPv-FtS_8DyOgAxs0130_provenance.
- NP85743.RAuroSg7Mday4I3_bJOQ7eQDirzMoIWBsFR2pe3FF52a4130_assertion description "[An interleukin-6 gene promoter polymorphism influences the biological phenotype of ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85743.RAuroSg7Mday4I3_bJOQ7eQDirzMoIWBsFR2pe3FF52a4130_provenance.
- NP85747.RAiY0uj0O0Py40g0QJ_0JbXmJgLxfQeVv2iYbIrhpXFfA130_assertion description "[Gene IL6 G(-174)C and gene IL10 G(-1082)A polymorphisms are associated with unfavourable outcomes in patients with acute coronary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85747.RAiY0uj0O0Py40g0QJ_0JbXmJgLxfQeVv2iYbIrhpXFfA130_provenance.
- NP85750.RAtEpVWtYBTLq3FZOncJZzn2ZCzcmIIptBvSmZzEjgmRI130_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." NP85750.RAtEpVWtYBTLq3FZOncJZzn2ZCzcmIIptBvSmZzEjgmRI130_provenance.
- NP85756.RArKO9RLjkw7foEDoBWCh2_ALg3XzSk4Qxkpc9o2xsqhc130_assertion description "[Cytokine polymorphisms and Alzheimer disease: possible associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85756.RArKO9RLjkw7foEDoBWCh2_ALg3XzSk4Qxkpc9o2xsqhc130_provenance.
- NP85758.RAmK7Zr8QCc2eSbXmHs7EZ4zuFihlgGZAwt9T0K2sSR4Q130_assertion description "[These results suggest that CACNA1C may be associated with secondary hyperparathyroidism. In addition, the haplotype-based approach may be useful to screen for key molecules associated with complex traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85758.RAmK7Zr8QCc2eSbXmHs7EZ4zuFihlgGZAwt9T0K2sSR4Q130_provenance.
- NP85765.RArSxt5bJvOzlp_mPsMk3t6eA7eBj7dCoxLIOcyZ4Dfe0130_assertion description "[Significant associations between alleles, genotypes, and haplotypes of polymorphisms in the IL4 gene and chronic periodontitis were verified in Brazilian individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85765.RArSxt5bJvOzlp_mPsMk3t6eA7eBj7dCoxLIOcyZ4Dfe0130_provenance.
- NP85794.RAgDrbOhRcwvi_rhfyh-LdTTRd_8qabENHZ1mh-4gsU3s130_assertion description "[Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85794.RAgDrbOhRcwvi_rhfyh-LdTTRd_8qabENHZ1mh-4gsU3s130_provenance.
- NP85796.RAmF1qv8EXEegd1ceBlgrA-Jpm24kZSI4tngci1M0x20g130_assertion description "[Results of this study support an immune-related etiology of childhood ALL. Further confirmation is required to detect functional variants in the significant genomic regions identified in this study, in particular for IL12A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85796.RAmF1qv8EXEegd1ceBlgrA-Jpm24kZSI4tngci1M0x20g130_provenance.
- NP85813.RAq4V0jwT452qT6qLX6YEwi9ZCS2IznwfIihYGIrQxDQI130_assertion description "[Association of interleukin-1 beta (-511C/T) polymorphisms with osteoporosis in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85813.RAq4V0jwT452qT6qLX6YEwi9ZCS2IznwfIihYGIrQxDQI130_provenance.
- NP85816.RArQ9yD4Euq6px3pBymdvjh3GUGyjLHMsRwahSkXzgCic130_assertion description "[Po-husk, apart from lowering LDL-C, also reduced TG, TG related to certain gene variants, TC, Apo B-100, oxLDL, insulin-resistance and systolic BP in mild-moderate hypercholesterolaemic individuals. Thus, the target patients to receive Po-husk would be those who present a cluster of various CVD risk factors, such as metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85816.RArQ9yD4Euq6px3pBymdvjh3GUGyjLHMsRwahSkXzgCic130_provenance.
- NP85818.RAi_0oJlpnIyjgkXAPCNC73Tm6CFKFzNRtPKeflBKxvC8130_assertion description "[Genetically elevated apolipoprotein A-I, high-density lipoprotein cholesterol levels, and risk of ischemic heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85818.RAi_0oJlpnIyjgkXAPCNC73Tm6CFKFzNRtPKeflBKxvC8130_provenance.
- NP85821.RAh3OOBaOYk7zioNZsaA6uHp9QtflDCYQfG5cCRNr_bPQ130_assertion description "[We sought to determine whether the proinflammatory M694V mutation of pyrin, the gene responsible for familial Mediterranean fever, could lead to an increased risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85821.RAh3OOBaOYk7zioNZsaA6uHp9QtflDCYQfG5cCRNr_bPQ130_provenance.
- NP85825.RAva-lMQL2lN6BpxLChUEvFa2uB10Z1zF9pXBdv4mGZO4130_assertion description "[MCPH1 and abnormal spindle-like MCPH associated (ASPM) are the two known MCPH causing genes that were suggested undergone recent positive selection in human populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85825.RAva-lMQL2lN6BpxLChUEvFa2uB10Z1zF9pXBdv4mGZO4130_provenance.
- NP85827.RArLL0j9q-08z8CiVo537i5dA2ZwlQZBJKj0jBRIM7XLk130_assertion description "[Polymorphisms in candidate genes and risk of scarring trachoma in a Chlamydia trachomatis--endemic population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85827.RArLL0j9q-08z8CiVo537i5dA2ZwlQZBJKj0jBRIM7XLk130_provenance.
- NP85832.RArNhDciu6axF0mheq4n6Y0X2n1XzGRm6ysOzMwyWw3R4130_assertion description "[This study indicates the important role of variant MBL alleles in the susceptibility to asthma in children infected with C pneumoniae.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85832.RArNhDciu6axF0mheq4n6Y0X2n1XzGRm6ysOzMwyWw3R4130_provenance.
- NP85833.RAnJ2cG92Ac4ZKvkR1phcP8-xaPMagdhwMf5Ogo_fixpM130_assertion description "[Mannose-binding lectin 2 (MBL2) gene polymorphism in asthma and atopy among adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85833.RAnJ2cG92Ac4ZKvkR1phcP8-xaPMagdhwMf5Ogo_fixpM130_provenance.
- NP85841.RAvRIrk4jQmzV_ZYyG0vi2eC2f8MPjMT0Kf37o3N3h3Ws130_assertion description "[There was, however, no association between MBL genotypes, which are associated with low or deficient serum levels of MBL, and mortality related to SARS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85841.RAvRIrk4jQmzV_ZYyG0vi2eC2f8MPjMT0Kf37o3N3h3Ws130_provenance.
- NP85845.RAhUGab55d-y06mh6s85NaBSpNIgDRjQjU8-sFtbdG9rU130_assertion description "[Genotypes resulting in high levels of MBL were more frequent (odds ratio OR, 2.5 95% confidence interval CI, 1.3-5.0; P=.006) among individuals with VL than among those with asymptomatic infections and were even more frequent (OR, 3.97 95% CI, 1.10-14.38; P=.043) among cases of VL presenting with clinical complications than among those with uneventful courses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85845.RAhUGab55d-y06mh6s85NaBSpNIgDRjQjU8-sFtbdG9rU130_provenance.
- NP85851.RAgROi5b6h5o45vlhtaLwGYET1DELWV9pK_tvubYTcrE4130_assertion description "[The distributions of the HY/HY, HY/LY, LY/LY, and LY/LX genotypes of MBL2 gene promoter and 119C>A genotype of the TLR4 gene were similar in patients with mild or severe acute pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85851.RAgROi5b6h5o45vlhtaLwGYET1DELWV9pK_tvubYTcrE4130_provenance.
- NP85853.RAltuEal7vu3q3Eda7p1USeKQRS0YTPC5n17zX7vcD4w0130_assertion description "[The tau H2 haplotype is almost exclusively Caucasian in origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85853.RAltuEal7vu3q3Eda7p1USeKQRS0YTPC5n17zX7vcD4w0130_provenance.
- NP85863.RAkcQPr7yWXG1UYkElx_40Z4J3wJ_L4T-G6JIuvXBe3zI130_assertion description "[Although the observed association of SMAD7 and KLF10 gene variants with T2D is modest, they may weakly contribute to a particular genetic background that increases the susceptibility to development of T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85863.RAkcQPr7yWXG1UYkElx_40Z4J3wJ_L4T-G6JIuvXBe3zI130_provenance.
- NP85870.RApqPplVgjnn3tgS_UzPkrOrV7dp28OeZaMAkKLbvEJX4130_assertion description "[High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85870.RApqPplVgjnn3tgS_UzPkrOrV7dp28OeZaMAkKLbvEJX4130_provenance.
- NP85871.RAg3W265DLsrNQhodnbrM1ouzT9iS4LXp7JfWoNFqEEMU130_assertion description "[We focused on two biologically relevant gene categories: genes involved in non-HFE GH (TFR2, HAMP, and SLC40A1) and genes involved in the regulation of hepcidin expression, including genes from the bone morphogenetic protein (BMP) regulatory pathway (BMP2, BMP4, HJV, SMAD1, SMAD4, and SMAD5) and the IL6 gene from the inflammation-mediated regulation pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85871.RAg3W265DLsrNQhodnbrM1ouzT9iS4LXp7JfWoNFqEEMU130_provenance.
- NP85875.RAieQ-Zhj-ZYATYyC3HmKFkpXLm35wryhea0wMw2i_ZW4130_assertion description "[The gene polymorphism of tumor necrosis factor-beta, but not that of tumor necrosis factor-alpha, is associated with the prognosis of sarcoidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85875.RAieQ-Zhj-ZYATYyC3HmKFkpXLm35wryhea0wMw2i_ZW4130_provenance.
- NP85877.RAqBFFkD3-S9CN9Dk4Zylo-44BSHseb9jQv_kMYW1bsHM130_assertion description "[Recurrent miscarriage and variant alleles of mannose binding lectin, tumour necrosis factor and lymphotoxin alpha genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85877.RAqBFFkD3-S9CN9Dk4Zylo-44BSHseb9jQv_kMYW1bsHM130_provenance.
- NP85879.RAjXwflY-EFUAn-Kb2ut6-i12WxA1HHj_0QwBTNDvSTTE130_assertion description "[TNF alpha and LT alpha gene polymorphisms as additional markers of celiac disease susceptibility in a DQ2-positive population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85879.RAjXwflY-EFUAn-Kb2ut6-i12WxA1HHj_0QwBTNDvSTTE130_provenance.
- NP85883.RAnerOGQfczvGCEWwof5B58QOlW0-TUnYa71BYzbQW0Gc130_assertion description "[Tumor necrosis factor-beta gene polymorphism may not be associated with major depressive disorder in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85883.RAnerOGQfczvGCEWwof5B58QOlW0-TUnYa71BYzbQW0Gc130_provenance.
- NP85888.RAi3WnnLmOaSzaYD-qbOdex8_Cr6DrzD4W_eg4U47NSqo130_assertion description "[Polymorphisms within the tumor necrosis factor and lymphotoxin-alpha genes and endemic pemphigus foliaceus--are there any associations?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85888.RAi3WnnLmOaSzaYD-qbOdex8_Cr6DrzD4W_eg4U47NSqo130_provenance.
- NP85891.RAigEVVKmzlOfgda_-YyZ-Pm0cpMViUmkqQhc8xFg-9Y4130_assertion description "[IL-10 and TNF-beta gene polymorphisms have no major influence on lactate levels after cardiac surgery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85891.RAigEVVKmzlOfgda_-YyZ-Pm0cpMViUmkqQhc8xFg-9Y4130_provenance.
- NP85892.RAt9X14c_HpNjWK7L5UevKPjHs4e9tZbiYjkXwG7hYRhU130_assertion description "[LTA 252G allele containing haplotype block is associated with high serum C-reactive protein levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85892.RAt9X14c_HpNjWK7L5UevKPjHs4e9tZbiYjkXwG7hYRhU130_provenance.
- NP85895.RAkFFgQYi4pFGDkUBo2WmBNkYFBj5kpYcfhxbhFbUTBtE130_assertion description "[The IL-6 G-174C polymorphism may be associated with ischaemic stroke in patients without a history of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85895.RAkFFgQYi4pFGDkUBo2WmBNkYFBj5kpYcfhxbhFbUTBtE130_provenance.
- NP85899.RAssFKDH75R3yLk23tFDWZBW9pbpGijZUfMyvfTpGVHME130_assertion description "[Homozygosity with respect to the LTA +80C and LTA +252G alleles was significantly more frequent in the patients with CCC than in the ASY patients (homozygosity for LTA +80C, 47% vs. 33%; homozygosity for LTA +252G, 16% vs. 8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85899.RAssFKDH75R3yLk23tFDWZBW9pbpGijZUfMyvfTpGVHME130_provenance.
- NP85914.RAoOA7wkEAl5EqXmFLj1H8WLPEd3Uk-JbZ7LPzbrXjb8I130_assertion description "[Hepatic lipase C-480T genotype-dependent benefit from long-term hormone replacement therapy for atherosclerosis progression in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85914.RAoOA7wkEAl5EqXmFLj1H8WLPEd3Uk-JbZ7LPzbrXjb8I130_provenance.
- NP85924.RAjlocrRXKZ5OuWq4wej56d9Ezx4z4EtLlcKaLWUIXmxk130_assertion description "[The gene frequencies of ACE, G-protein, ecNOS, Leptin and UCP2 in 184 ESRD patients and 569 healthy controls from North India were compared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85924.RAjlocrRXKZ5OuWq4wej56d9Ezx4z4EtLlcKaLWUIXmxk130_provenance.
- NP85926.RArAOpKo_zTtYgarMojvwpHi22xQ0QyGIccdkKX24iPc8130_assertion description "[The identification of a novel missense mutation in only one of the patients implied that TCF8 does not play a significant role in the pathogenesis of FECD in this Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85926.RArAOpKo_zTtYgarMojvwpHi22xQ0QyGIccdkKX24iPc8130_provenance.
- NP85939.RAqRdVUXL9rBKVEPudxdsZdz1pMK1RrMcah6dVYHiruIQ130_assertion description "[, we demonstrated an association between D2080N polymorphism with factor VIII and von Willebrand factor levels in Brazilian normal individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85939.RAqRdVUXL9rBKVEPudxdsZdz1pMK1RrMcah6dVYHiruIQ130_provenance.
- NP85940.RAv67c76tdC8W5-eXkElF5mKEdTmr3yTFGgs7nzT0CP7w130_assertion description "[A rapid and reliable detection system for identifying mitochondrial polymorphisms and haplotypes was developed based on hybridization probe technology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85940.RAv67c76tdC8W5-eXkElF5mKEdTmr3yTFGgs7nzT0CP7w130_provenance.
- NP85941.RArceYbxliwoyMCZu7OuKhIizADiryn1mxD1wiNKJCphk130_assertion description "[A mitochondrial DNA variant at position 16189 is associated with type 2 diabetes mellitus in Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85941.RArceYbxliwoyMCZu7OuKhIizADiryn1mxD1wiNKJCphk130_provenance.
- NP85943.RAo1VjhdjNYwLTsxmOR4amY9hRSvyIcx8jzFykcZhifuA130_assertion description "[Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85943.RAo1VjhdjNYwLTsxmOR4amY9hRSvyIcx8jzFykcZhifuA130_provenance.
- NP85947.RAsRq0Umd3GWMmkM3zwVnpxJhQt8OECak2Bx_5LGQVWKE130_assertion description "[TGF-beta1 and TSC-22 gene polymorphisms and susceptibility to microvascular complications in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85947.RAsRq0Umd3GWMmkM3zwVnpxJhQt8OECak2Bx_5LGQVWKE130_provenance.
- NP85954.RAqSTUkF9vOvnCrkvdUsOUOKGMHXR1weqXqUNPRrYERQk130_assertion description "[Mutation scanning of the androgen receptor gene in patients with psychiatric disorders reveals highly conserved variants in alcoholic and phobia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85954.RAqSTUkF9vOvnCrkvdUsOUOKGMHXR1weqXqUNPRrYERQk130_provenance.
- NP85955.RAuZTzIMrpnc2qaxKZdSBFyK5yN0xvvjJ8BI57Mf4ceP4130_assertion description "[The CAG repeat polymorphism in the androgen receptor gene is associated with HDL-cholesterol but not with coronary atherosclerosis or myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85955.RAuZTzIMrpnc2qaxKZdSBFyK5yN0xvvjJ8BI57Mf4ceP4130_provenance.
- NP85959.RAgxmLBbRgSUBM1Q9v5aY5EYwIyhE0RA8P2fnJpdSUWxM130_assertion description "[The androgen receptor gene CAG repeat polymorphism does not predict increased risk of heart disease: longitudinal results from the Massachusetts Male Ageing Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85959.RAgxmLBbRgSUBM1Q9v5aY5EYwIyhE0RA8P2fnJpdSUWxM130_provenance.
- NP85965.RAkHTPlcd7jPx14gfEvECifKIip0Io4gzb8JBXeRLob_E130_assertion description "[, the DD genotype of the ACE gene impairs the coronary release of tPA induced by BK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85965.RAkHTPlcd7jPx14gfEvECifKIip0Io4gzb8JBXeRLob_E130_provenance.
- NP85970.RAg3opWrQfg5JofMCFtyEYg0NHiGvPiPDSfAyJNp0-qLs130_assertion description "[No association of KIR genes with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85970.RAg3opWrQfg5JofMCFtyEYg0NHiGvPiPDSfAyJNp0-qLs130_provenance.
- NP85973.RAlGLcRZ0Wx3u2Y31VSr7WLKcawWeOE0PSEI-Q0yQgBMA130_assertion description "[We investigated killer cell immunoglobulin-like receptor (KIR) genotypes in 92 patients with young-onset type 1 diabetes mellitus (YT1DM: < or =35 years old), 112 patients with adult-onset type 1 diabetes mellitus (AT1DM: >35 years old) and 240 control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85973.RAlGLcRZ0Wx3u2Y31VSr7WLKcawWeOE0PSEI-Q0yQgBMA130_provenance.
- NP85980.RAqMDNj3_IW85bwLdW8CO3ULjb-dG-hy0ZN-a6nK9agWg130_assertion description "[No association of KIR genes with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85980.RAqMDNj3_IW85bwLdW8CO3ULjb-dG-hy0ZN-a6nK9agWg130_provenance.
- NP85982.RAijL92SO6zw8eM-W-TtheVRpbHeo3sQ0o8yeW4u5HUp0130_assertion description "[No association of KIR genes with Behcet's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85982.RAijL92SO6zw8eM-W-TtheVRpbHeo3sQ0o8yeW4u5HUp0130_provenance.
- NP85987.RAllyv2gOzD_Iz8izTfOTsWb-R3rNB5BszXoukHDkFLi8130_assertion description "[These results do not show a significant role for the tested candidate gene variants and also do not support the hypothesis that a common chromosome 1 defective gene influences both FHM and the more common forms of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85987.RAllyv2gOzD_Iz8izTfOTsWb-R3rNB5BszXoukHDkFLi8130_provenance.
- NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_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." NP85988.RAn935k9YTV293cxPO7TbhPx-OEdAJaXAPbXA89PN3pqM130_provenance.
- NP85995.RAhlC6_VQKLzRoAlwiTw82ONgfTQgS7UUJptVAqRdZ0p0130_assertion description "[Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85995.RAhlC6_VQKLzRoAlwiTw82ONgfTQgS7UUJptVAqRdZ0p0130_provenance.
- NP85998.RAsMkflEFCz7GQ6pNVooZhBw7QmGSUp8CTnNR19XvxjlI130_assertion description "[Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85998.RAsMkflEFCz7GQ6pNVooZhBw7QmGSUp8CTnNR19XvxjlI130_provenance.
- NP86000.RAv9LNg8ela3WpEv4nyeNHBbBgzJsRIF4syqGZeDxrws4130_assertion description "[Apolipoprotein E polymorphisms and age at first coronary artery bypass graft.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86000.RAv9LNg8ela3WpEv4nyeNHBbBgzJsRIF4syqGZeDxrws4130_provenance.
- NP86012.RAmr_V_lKvBpvE6pnbYemxhOlhXP4T-l_f7TxGyrXObLg130_assertion description "[APOE 4 is a risk factor for cerebral infarction among the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86012.RAmr_V_lKvBpvE6pnbYemxhOlhXP4T-l_f7TxGyrXObLg130_provenance.
- NP86013.RAuXVdIPLcv64TvwYeYAdZtxp5p49JX307cqtawcWfe7U130_assertion description "[Candidate genes of cerebral infarction and traditional classification in Koreans with cerebral infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86013.RAuXVdIPLcv64TvwYeYAdZtxp5p49JX307cqtawcWfe7U130_provenance.
- NP86017.RAiJhL3PXLdgZNKb5dHcvBWwOLisBOlrrVkw_ejXiL-bQ130_assertion description "[) of onset of pSS in all apoE epsilon4 allele carriers was 46 +/- 12 and in other genotypes it was 53 +/- 10 yr (P = 0.031, t-test).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86017.RAiJhL3PXLdgZNKb5dHcvBWwOLisBOlrrVkw_ejXiL-bQ130_provenance.
- NP86021.RAj558_8rGoGXTXbo17ZFxULcm1UnG3xLMJcl2p26aOMM130_assertion description "[However, the APOE impact on cognitive development in children living in poor areas of the developing world, where we have discovered profound significant associations of early childhood diarrhea (at 0-2 y) with lasting impairments of growth, cognition, and school performance, is not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86021.RAj558_8rGoGXTXbo17ZFxULcm1UnG3xLMJcl2p26aOMM130_provenance.
- NP86022.RAmlbROONtB_lydD7IBfdsTS6HPMlenqMpbbnBbW_bV48130_assertion description "[Apolipoprotein E, B vitamins, and cognitive function in older adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86022.RAmlbROONtB_lydD7IBfdsTS6HPMlenqMpbbnBbW_bV48130_provenance.
- NP86023.RAoIdoQUa04UzY7GAV6Nv0XDVzoUoxMwn3YqEZZFbsfYg130_assertion description "[An association of allele epsilon 2 of apoE gene with the maturation of HDL in type IV hyperlipidemia was noted in the study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86023.RAoIdoQUa04UzY7GAV6Nv0XDVzoUoxMwn3YqEZZFbsfYg130_provenance.
- NP86025.RAqQcqDzid-BWg0feLnqpFvWTlfE-zi5wz9M4hrWu4btg130_assertion description "[Hypotension is an important factor for performance on the MMSE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86025.RAqQcqDzid-BWg0feLnqpFvWTlfE-zi5wz9M4hrWu4btg130_provenance.
- NP86032.RAghR7F7SyHn1ZfaaYYefMFxAHgqHTsZMnwazVNszHWRw130_assertion description "[The relationship between apolipoprotein E polymorphism, lipoprotein (a) and fatty liver disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86032.RAghR7F7SyHn1ZfaaYYefMFxAHgqHTsZMnwazVNszHWRw130_provenance.
- NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion description "[APOE epsilon4 allele is more frequent in children with obstructive sleep apnea and particularly in those who develop neurocognitive deficits, suggesting that the APOE epsilon4 allele is associated with not only increased odds of having sleep-disordered breathing, but also with an increased risk for neurocognitive dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance.
- NP86039.RApWtxV5qUfjjI0X2VKWrXxiMkO5vob-89l_hJumw9mUw130_assertion description "[Apolipoprotein E epsilon4 allele is associated with the volume of white matter changes in patients with lacunar infarcts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86039.RApWtxV5qUfjjI0X2VKWrXxiMkO5vob-89l_hJumw9mUw130_provenance.
- NP86040.RAt_7FCffec7wn2YFGbVTi-SVinAA6MYR88TB9grsXmdM130_assertion description "[The present study indicates that in the Ouro Preto admixed population the presence of APOE *2 can confer a protective effect, whereas the presence of APOE *4 implies an enhanced risk for dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86040.RAt_7FCffec7wn2YFGbVTi-SVinAA6MYR88TB9grsXmdM130_provenance.
- NP86041.RAnI0AQhA6LAb4IzM8uf2YHK6oRj4HGBB3mWO6vLjQbzI130_assertion description "[Our findings argue against a specific role for any APOE alleles in conferring susceptibility to sIBM but have demonstrated a non-significant trend towards an earlier age-of-onset in patients with the epsilon2 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86041.RAnI0AQhA6LAb4IzM8uf2YHK6oRj4HGBB3mWO6vLjQbzI130_provenance.
- NP86048.RArpGoT-iDfu7yHT2tfVKA0yizDvWqa-6BNvSn2GC_t4A130_assertion description "[Decrease of insulin sensitivity and increase of insulin resistance are more obvious in hypertensive patients with genotype G of the 3 genes of SM constitution than in those of PI constitution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86048.RArpGoT-iDfu7yHT2tfVKA0yizDvWqa-6BNvSn2GC_t4A130_provenance.