Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP86771.RAvcxnCtGbcaQG5yzUzurwHSzuFUjNLRy6Dxesg_VplSc130_assertion description "[Characterization of tumor necrosis factor- block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86771.RAvcxnCtGbcaQG5yzUzurwHSzuFUjNLRy6Dxesg_VplSc130_provenance.
- NP86777.RAhJqwx9V8sZAfKnssOaaqv-pULTtZ1qiCI1Kh7ONXVV8130_assertion description "[Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86777.RAhJqwx9V8sZAfKnssOaaqv-pULTtZ1qiCI1Kh7ONXVV8130_provenance.
- NP86780.RArAa162ruRQIB4HIRM5FSpufwoyuSqwm88-e0fyPVsSo130_assertion description "[These data suggest that genes located within the MHC may play a role in the susceptibility to Poncets disease in patients diagnosed with TB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86780.RArAa162ruRQIB4HIRM5FSpufwoyuSqwm88-e0fyPVsSo130_provenance.
- NP86781.RAvzxMxJwZMmjweUGJFPsLZlb3zDDGcqPfd1npweBv1dU130_assertion description "[The aim of this study was to determine whether specific alleles in the human leukocyte antigen (HLA)-DRB1 and HLA-DQB1 genes correlated with NTG in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86781.RAvzxMxJwZMmjweUGJFPsLZlb3zDDGcqPfd1npweBv1dU130_provenance.
- NP86782.RAnNG8wdmFVixzIW3D_seSnh302XwLgALvyQEWDk6zS5I130_assertion description "[Association analysis about HLA-DRB1, -DQB1 polymorphism and auto-antibodies against (1)-adrenergic receptors in Chinese patients with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86782.RAnNG8wdmFVixzIW3D_seSnh302XwLgALvyQEWDk6zS5I130_provenance.
- NP86793.RAjUkURaITpLUcBTcy0puLGqsCMxF4B-3pTqok85k_uUg130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86793.RAjUkURaITpLUcBTcy0puLGqsCMxF4B-3pTqok85k_uUg130_provenance.
- NP86794.RAggDrlrxA2TRzfCrtDwl0PbLZyH0NDI26k0x6gjOgu7A130_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." NP86794.RAggDrlrxA2TRzfCrtDwl0PbLZyH0NDI26k0x6gjOgu7A130_provenance.
- NP86802.RAorOTK2lIaWItLosHm8HWbV_eKnBf-LBeNNlSf7fzO8g130_assertion description "[HLA-B alleles showed fast off-rates in peptide binding and restricted high numbers (up to 6%) of antigen-specific CD8+ T cells in patients with pulmonary tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86802.RAorOTK2lIaWItLosHm8HWbV_eKnBf-LBeNNlSf7fzO8g130_provenance.
- NP86803.RAjKkHFE_KyZE6w2zlepHz8NK1moz2zojU_RCl-1QnrKE130_assertion description "[Epidemiological data were consistent with previously reported studies. There appears to be no association between the occurrence of pars planitis and HLA DR 15 or other known HLA genotypes in Spanish patients. However, the small sample size could have limited the power of this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86803.RAjKkHFE_KyZE6w2zlepHz8NK1moz2zojU_RCl-1QnrKE130_provenance.
- NP86806.RAh6nvY0ItM-uQ1ZAs6MzHyLcsT9or_MvR0n1cfnOVuQI130_assertion description "[HLA polymorphisms in Italian children with autism spectrum disorders: results of a family based linkage study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86806.RAh6nvY0ItM-uQ1ZAs6MzHyLcsT9or_MvR0n1cfnOVuQI130_provenance.
- NP86810.RAlwHA3tObsmZ_DNAv2P81F32TfuNNDEdvUnSLo_Oa1aA130_assertion description "[Affinity (ED(50)) and half-life (t(1/2), off-rate) analysis for individual peptide species on HLA-A and HLA-B molecules revealed binding ranges between 10(-3) and 10(-7) M. After selection of the best matches, major histocompatibility complex class I/peptide tetramer complexes were constructed to measure the CD8+ T-cell responses directly ex vivo in peripheral blood mononuclear cells (PBMC) derived from 57 patients with acute pulmonary tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86810.RAlwHA3tObsmZ_DNAv2P81F32TfuNNDEdvUnSLo_Oa1aA130_provenance.
- NP86811.RAptTmI8Z4USihgn1hH7CGzlGjD9TIhMRqhrzDfJUnUHU130_assertion description "[Epidemiological data were consistent with previously reported studies. There appears to be no association between the occurrence of pars planitis and HLA DR 15 or other known HLA genotypes in Spanish patients. However, the small sample size could have limited the power of this study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86811.RAptTmI8Z4USihgn1hH7CGzlGjD9TIhMRqhrzDfJUnUHU130_provenance.
- NP86813.RAufJZGd0aAl8gWQ41pqpZBUF_9vhSeRalmCbYVNwJjkc130_assertion description "[Enhanced susceptibility of HLA-mediated ticlopidine-induced idiosyncratic hepatotoxicity by CYP2B6 polymorphism in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86813.RAufJZGd0aAl8gWQ41pqpZBUF_9vhSeRalmCbYVNwJjkc130_provenance.
- NP86817.RAqP7iUu6fUNA7Ugkef9Jj9K9X_mRH4uwvfsVic079cQU130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86817.RAqP7iUu6fUNA7Ugkef9Jj9K9X_mRH4uwvfsVic079cQU130_provenance.
- NP86824.RAipkO6cTV5WBvCAOtgLKOA44xVjde21vTp1LDFrY5x_0130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86824.RAipkO6cTV5WBvCAOtgLKOA44xVjde21vTp1LDFrY5x_0130_provenance.
- NP86825.RApH5ih_1akSMsPM8rxtE14lr5L6WtFqMgN6uGWMAcjRE130_assertion description "[MicroRNAs and target site screening reveals a pre-microRNA-30e variant associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86825.RApH5ih_1akSMsPM8rxtE14lr5L6WtFqMgN6uGWMAcjRE130_provenance.
- NP86826.RAm0wmV2SZsqEQiJo-a_xdms23-DCwRYKXssoNC3zzuKs130_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." NP86826.RAm0wmV2SZsqEQiJo-a_xdms23-DCwRYKXssoNC3zzuKs130_provenance.
- NP86830.RAq-vjg9WeuSi6COvG5QuvmFWQSrmFuEyVHyy4A-lH0k4130_assertion description "[We confirm that 5 genetic regions associated with lipid traits in European-derived populations are relevant in African Americans. To further evaluate these loci, fine-mapping in larger African American cohorts and/or resequencing will be required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86830.RAq-vjg9WeuSi6COvG5QuvmFWQSrmFuEyVHyy4A-lH0k4130_provenance.
- NP86833.RAqf1gIIIKd91FBNXGl7sUrFbmkoRpn3M224BiQc14BPY130_assertion description "[The results demonstrated that genetic variation in KCNJ11, BDNF, PFKP, PTER and SEC16B were associated with SGA and support the concept that genetic factors associated with obesity and/or type 2 diabetes are more prevalent in those born SGA compared to those born AGA. We have previously determined that environmental factors are associated with differences in birthweight in the ABC study and now we have demonstrated a significant genetic contribution, suggesting that the interaction between genetics and the environment are important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86833.RAqf1gIIIKd91FBNXGl7sUrFbmkoRpn3M224BiQc14BPY130_provenance.
- NP86840.RAu7iqU7HJDRs2razOfjMj-ervgMKMoktCjf2wq6RPMxs130_assertion description "[HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86840.RAu7iqU7HJDRs2razOfjMj-ervgMKMoktCjf2wq6RPMxs130_provenance.
- NP86846.RAoU0xpKrFrx-2PtZP_Rx5dc5WHqR6BgL203Pfwbz7ssI130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86846.RAoU0xpKrFrx-2PtZP_Rx5dc5WHqR6BgL203Pfwbz7ssI130_provenance.
- NP86850.RAr_E1YZ9yRqt2cRjIj2_g4Q04G8TeibLF0flBhAAMeQg130_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." NP86850.RAr_E1YZ9yRqt2cRjIj2_g4Q04G8TeibLF0flBhAAMeQg130_provenance.
- NP86866.RAjm-ArcKLPT3_l5IJHMVMYXwo8uiw5VWblrJ0d34RpyY130_assertion description "[Use of genome-wide expression data to mine the `Gray Zone` of GWA studies leads to novel candidate obesity genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86866.RAjm-ArcKLPT3_l5IJHMVMYXwo8uiw5VWblrJ0d34RpyY130_provenance.
- NP86871.RAu-5JltF2M5zwVTU8BKZuF5mgsazkokyfKRigPrNIZgA130_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." NP86871.RAu-5JltF2M5zwVTU8BKZuF5mgsazkokyfKRigPrNIZgA130_provenance.
- NP86874.RAnrZyJyd7LR1gGPdpLRruh83Y0QB7n_IEQCAogm8OfF0130_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." NP86874.RAnrZyJyd7LR1gGPdpLRruh83Y0QB7n_IEQCAogm8OfF0130_provenance.
- NP86884.RAhSv2t81qfXBqgODTMBf_Ypx5rBkZIuvIVZCmYjNdKtM130_assertion description "[Recent genome-wide and candidate gene studies of COPD implicate genetic variants on the chromosomal 4q31 (HHIP/glycophorin A (GYPA)) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86884.RAhSv2t81qfXBqgODTMBf_Ypx5rBkZIuvIVZCmYjNdKtM130_provenance.
- NP86886.RAh4PMeaeHoQ1ZMCuqSV3h5DA80VJDHTVennU16xGfYLY130_assertion description "[Variants in FAM13A are associated with chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86886.RAh4PMeaeHoQ1ZMCuqSV3h5DA80VJDHTVennU16xGfYLY130_provenance.
- NP86892.RArQ0HRcrPuV3mN63HfSqmjp9jPqL9Ix3bXoJ6pQwk690130_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." NP86892.RArQ0HRcrPuV3mN63HfSqmjp9jPqL9Ix3bXoJ6pQwk690130_provenance.
- NP86894.RAlZlgW0xV5R1kCtzJDWrZyXn4TBlUtKW9rfp8jHQUZUI130_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." NP86894.RAlZlgW0xV5R1kCtzJDWrZyXn4TBlUtKW9rfp8jHQUZUI130_provenance.
- NP86900.RAqr3ehpr7z6qjh3SVnod2_OF7wSvDo5uCy-SsHjvmz8o130_assertion description "[A comprehensive analysis of phase I and phase II metabolism gene polymorphisms and risk of non-small cell lung cancer in smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86900.RAqr3ehpr7z6qjh3SVnod2_OF7wSvDo5uCy-SsHjvmz8o130_provenance.
- NP86911.RAtfqqDdYUPRCj79WStYLxJVyjlosKt9yG3Ha0MF2EVss130_assertion description "[Using a multiplex polymerase chain reaction (PCR), GSTM1 and GSTT1 gene polymorphisms were analyzed in 195 patients with age-related cataract (75 patients with cortical, 53 with nuclear, 37 with posterior subcapsular, and 30 with mixed type) and in 136 patients of an otherwise healthy control group of similar age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86911.RAtfqqDdYUPRCj79WStYLxJVyjlosKt9yG3Ha0MF2EVss130_provenance.
- NP86912.RAo_XV3IiMCVBnarLbjeuBNucHibNFet6E7P4U3-_1PeQ130_assertion description "[Our results suggest that ESR1 gene polymorphisms may be associated with dysmenorrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86912.RAo_XV3IiMCVBnarLbjeuBNucHibNFet6E7P4U3-_1PeQ130_provenance.
- NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_assertion description "[Association of deletion polymorphism in GSTT1 and GSTM1 genes and polymorphic variant A313G of GSTP1 gene with cirrhosis diseases and 4-year survival rate for the Tomsk region (West Siberia) patients were tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86916.RAl0GKmpenr5M4eXyQaGwmrjRC-TNbMNuURMfFwLrsSV4130_provenance.
- NP86921.RAilwqsLGAUF7v-gpBvz7azkfeClc2hGAulptF5kcqq5Y130_assertion description "[No association was found between GSTT1 and GSTP1 polymorphisms and EA children or their mothers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86921.RAilwqsLGAUF7v-gpBvz7azkfeClc2hGAulptF5kcqq5Y130_provenance.
- NP86922.RAkcptUKR8UuK-bWkgsd0nwBdDdDCdFFcXgM34zcSBAGw130_assertion description "[The role of genetic determinant in the development of severe perinatal asphyxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86922.RAkcptUKR8UuK-bWkgsd0nwBdDdDCdFFcXgM34zcSBAGw130_provenance.
- NP86929.RAgXvBdieVZ2PYltsdrNje5KcVFZehYGvyurEr4Bfp8gk130_assertion description "[The findings are consistent with our hypothesis that variability in genes involved in steroidogenesis and estrogen metabolism may alter the risk of developing endometrial cancer, suggesting that they may be useful as biomarkers for genetic susceptibility to endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86929.RAgXvBdieVZ2PYltsdrNje5KcVFZehYGvyurEr4Bfp8gk130_provenance.
- NP86931.RAlPkwpIj-gA_4YHokz8_tDClv98opTeeKZPj_JZ36cU0130_assertion description "[Analysis of glutathione S-transferase Pi isoform (GSTP1) single-nucleotide polymorphisms and macular telangiectasia type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86931.RAlPkwpIj-gA_4YHokz8_tDClv98opTeeKZPj_JZ36cU0130_provenance.
- NP86933.RAvxv6bllxkOqSLLi948ccpnu9CyKo4IeCvNJiWsW_hVU130_assertion description "[Preliminary evidence of ethnic divergence in associations of putative genetic variants for methamphetamine dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86933.RAvxv6bllxkOqSLLi948ccpnu9CyKo4IeCvNJiWsW_hVU130_provenance.
- NP86938.RAjiaIfbKwHrHFLUEoU7ASV3Fb5IpB5aNTq96B70ZmulM130_assertion description "[No association was found between GSTT1 and GSTP1 polymorphisms and EA children or their mothers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86938.RAjiaIfbKwHrHFLUEoU7ASV3Fb5IpB5aNTq96B70ZmulM130_provenance.
- NP86942.RAuEle6rSTDQM0_Hp-Z70TQceoMeV5RiGoK0_u_5xbVmw130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86942.RAuEle6rSTDQM0_Hp-Z70TQceoMeV5RiGoK0_u_5xbVmw130_provenance.
- NP86943.RAkHYZL3d17SPlFoctN0V4xxkkZABjpWjHsPYkdVGlmZY130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86943.RAkHYZL3d17SPlFoctN0V4xxkkZABjpWjHsPYkdVGlmZY130_provenance.
- NP86945.RAm-i8WmBEIdjaWl4o414MQGI6lcVkK5RJnd5-nV4lRMg130_assertion description "[These results suggest that GSTM4 polymorphisms are biomarkers for the prediction of cisplatin response. ABCC4 polymorphisms, as well as GSTT1 copy number, may also help to predict cisplatin response, but further validation is required. These results represent a step toward the individualized chemotherapy of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86945.RAm-i8WmBEIdjaWl4o414MQGI6lcVkK5RJnd5-nV4lRMg130_provenance.
- NP86947.RAkdFcX5TyuftldmZty6cwVEoosEQitNcojRHgUPGx_Nw130_assertion description "[Association between the glutathione S-transferase M1 gene deletion and female methamphetamine abusers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86947.RAkdFcX5TyuftldmZty6cwVEoosEQitNcojRHgUPGx_Nw130_provenance.
- NP86948.RAjcAePfqQ7S8sITaGpsr5RrHlBVry4KI6HQhYJAWvxzQ130_assertion description "[This study demonstrated that patients carrying GST M1-null genotype may be susceptible to ADIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86948.RAjcAePfqQ7S8sITaGpsr5RrHlBVry4KI6HQhYJAWvxzQ130_provenance.
- NP86965.RAtR9pkSM8eeNPHS9S7CS-2ot7to8AId0OX0WVc_MCPAU130_assertion description "[odds ratios (ORs) for head and neck cancer were 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86965.RAtR9pkSM8eeNPHS9S7CS-2ot7to8AId0OX0WVc_MCPAU130_provenance.
- NP86969.RAsy2BNhoZX6BqlzV5UoA3IH0UbaW-ygrNq_tBEo3DpLM130_assertion description "[GSTM1-/GSTT1- (null) genotype may be one of the associated genetic factor for the increased risk of PTL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86969.RAsy2BNhoZX6BqlzV5UoA3IH0UbaW-ygrNq_tBEo3DpLM130_provenance.
- NP86972.RAmoRn1sGu3IZYn67zmlpwjLguN1sxPPlBbd-5x4u8shU130_assertion description "[Results suggest that the GSTM1(-/-) null genotype may play an important role in the development of EA during early embryogenesis as a consequence of altered detoxification processes both in children and in the mothers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86972.RAmoRn1sGu3IZYn67zmlpwjLguN1sxPPlBbd-5x4u8shU130_provenance.
- NP86975.RAuOwe_Y0CxtR5HxM1DqHAzTsocBPHrBYo728EX0OL2QQ130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86975.RAuOwe_Y0CxtR5HxM1DqHAzTsocBPHrBYo728EX0OL2QQ130_provenance.
- NP86980.RApYIa8ZTNl9fyL5AYU7bx45nNX4U-xJjJzWrLgoFPK58130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86980.RApYIa8ZTNl9fyL5AYU7bx45nNX4U-xJjJzWrLgoFPK58130_provenance.
- NP86983.RAiyQXcVxwYI8XSBG0kFjQv9ovrhKSa7-q-L-Zt0Dmq9E130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86983.RAiyQXcVxwYI8XSBG0kFjQv9ovrhKSa7-q-L-Zt0Dmq9E130_provenance.
- NP86990.RAuZwH_0l4nKwfHaOfL0GU-pT9vnXj-cRZeUWfH2c_21o130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86990.RAuZwH_0l4nKwfHaOfL0GU-pT9vnXj-cRZeUWfH2c_21o130_provenance.
- NP86992.RAs502uIOSFidM-ZVWh1DHP1TqJ0f9WKAVq1lJr5eUXDQ130_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." NP86992.RAs502uIOSFidM-ZVWh1DHP1TqJ0f9WKAVq1lJr5eUXDQ130_provenance.
- NP86999.RAj3ai0yMtTQWm8QVK3nrH5UyeCJ0wAree1-2FiUILp28130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86999.RAj3ai0yMtTQWm8QVK3nrH5UyeCJ0wAree1-2FiUILp28130_provenance.
- NP87005.RAqp3zOBUW51FDUwf56BnU4ZisdPgwdgxOHwvvYA8unwQ130_assertion description "[Although we have not been able to found a clear association between the studied CNVs and psychiatric disorders, the rare variants found only within the patients could account for a step further towards understanding the pathophysiology of psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87005.RAqp3zOBUW51FDUwf56BnU4ZisdPgwdgxOHwvvYA8unwQ130_provenance.
- NP87011.RAm7PmWoM9Go2l2u-UAHA_2wtu-Ed7GEmHZwg4TS96UIg130_assertion description "[A possible association of responsiveness to adrenocorticotropic hormone with specific GRIN1 haplotypes in infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87011.RAm7PmWoM9Go2l2u-UAHA_2wtu-Ed7GEmHZwg4TS96UIg130_provenance.
- NP87021.RAigvvctS0WsvpTTU6UVCniIz0ZffNeDy9ktlaQQLz83M130_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." NP87021.RAigvvctS0WsvpTTU6UVCniIz0ZffNeDy9ktlaQQLz83M130_provenance.
- NP87026.RAhilRjVciglLaV1d75nMIIoTMRAaggEacBuBoPcDRObA130_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." NP87026.RAhilRjVciglLaV1d75nMIIoTMRAaggEacBuBoPcDRObA130_provenance.
- NP87031.RAm6FQD_S_fbOSgRaprD6_xW4P09otQ4IVRmwYs-K0OEk130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87031.RAm6FQD_S_fbOSgRaprD6_xW4P09otQ4IVRmwYs-K0OEk130_provenance.
- NP87033.RAhseo9aUWJ46MVpGncHy36ie2707x2jC_D4kIwUWT6Pg130_assertion description "[These findings might help to explain biological effects of selenium in prostate cancer development in order to overcome inconsistencies arising from former studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87033.RAhseo9aUWJ46MVpGncHy36ie2707x2jC_D4kIwUWT6Pg130_provenance.
- NP87037.RAnsRJWtN0KJB0bMGKGqvNwgkjnTt9wYVXpSHE2XwlZiA130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87037.RAnsRJWtN0KJB0bMGKGqvNwgkjnTt9wYVXpSHE2XwlZiA130_provenance.
- NP87040.RAiAEFJBnhimyb7K14wUr5tuTBThy5vBkmp0mnNjA3WXA130_assertion description "[Genetic polymorphisms in apolipoprotein E and glutathione peroxidase 1 genes in the Ecuadorian population affected with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87040.RAiAEFJBnhimyb7K14wUr5tuTBThy5vBkmp0mnNjA3WXA130_provenance.
- NP87044.RAifu1NLiDPjtUrYl9PqxJP34rdn3Xnl9niYlpI3T324w130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87044.RAifu1NLiDPjtUrYl9PqxJP34rdn3Xnl9niYlpI3T324w130_provenance.
- NP87045.RAsYLhSwJXNkpoqF3oRXv59hK9mUE39UGS4p7R4l0k3os130_assertion description "[L41Q polymorphism of the G protein coupled receptor kinase 5 is associated with left ventricular apical ballooning syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87045.RAsYLhSwJXNkpoqF3oRXv59hK9mUE39UGS4p7R4l0k3os130_provenance.
- NP87051.RAt2c72BytIQCIy7nrp2LaZaxNPWPj1fjp9CiWDcuNpS8130_assertion description "[Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87051.RAt2c72BytIQCIy7nrp2LaZaxNPWPj1fjp9CiWDcuNpS8130_provenance.
- NP87054.RAmPYm4vseZNAd11lbo9ImHkQ7q0112KMDiNqSXKLieb0130_assertion description "[The results of our study indicate that genetic variation of F2 is associated with kidney stone risk in Northeastern Thai female patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87054.RAmPYm4vseZNAd11lbo9ImHkQ7q0112KMDiNqSXKLieb0130_provenance.
- NP87056.RAnlugrVMPV2ynsobcdKyr2SH31P7Vvzsg7KGmJ-d_7x8130_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." NP87056.RAnlugrVMPV2ynsobcdKyr2SH31P7Vvzsg7KGmJ-d_7x8130_provenance.
- NP87060.RAntlaftedUKUjJ2lhDMgNRslPepvQk2Vund38u5GiNqg130_assertion description "[Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87060.RAntlaftedUKUjJ2lhDMgNRslPepvQk2Vund38u5GiNqg130_provenance.
- NP87062.RAheXV9FJPDOTphTAxTopWEhmfKTQcdaMsrkssau5zZxI130_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." NP87062.RAheXV9FJPDOTphTAxTopWEhmfKTQcdaMsrkssau5zZxI130_provenance.
- NP87068.RAoKkLfPomLM1IFee6L5BoOd_dp4e0nIE818gW-v3d72E130_assertion description "[This study identified a novel locus associated with all-cause mortality among individuals of European ancestry with HF. This finding warrants additional investigation, including replication, in other studies of HF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87068.RAoKkLfPomLM1IFee6L5BoOd_dp4e0nIE818gW-v3d72E130_provenance.
- NP87073.RAij0temmzpzEObopEEryimW_HyAg34ODq6lmsIMkST64130_assertion description "[NKAIN2 showed suggestive evidence of association with neuroticism as a main effect (p < 10(-6)) and GPC6 showed suggestive evidence for interaction with age (p approximately = 10(-7)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87073.RAij0temmzpzEObopEEryimW_HyAg34ODq6lmsIMkST64130_provenance.
- NP87074.RAp02gDDD0qHAP_ajMHcbIxiEQIhcwM_XLIpyoeTSF3T4130_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." NP87074.RAp02gDDD0qHAP_ajMHcbIxiEQIhcwM_XLIpyoeTSF3T4130_provenance.
- NP87076.RAk0hy8Sdssj7Kj1y0J_rBu-bSc7_d1zpQqDCDZgTkEMk130_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." NP87076.RAk0hy8Sdssj7Kj1y0J_rBu-bSc7_d1zpQqDCDZgTkEMk130_provenance.
- NP87078.RAneWVYKimQLTrx6-I0bNwrEm2Mbrjla6ZasONgL5du4A130_assertion description "[The paucity of patient-specific missense mutations and contradictory findings with respect to 2 common polymorphisms in the 2 contrasting populations suggest that the GP2 gene is unlikely to play a major role in the etiology of chronic pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87078.RAneWVYKimQLTrx6-I0bNwrEm2Mbrjla6ZasONgL5du4A130_provenance.
- NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_assertion description "[, the 807T allele of GP Ia and the PlA2 allele of GP IIIa, and specially its combination, may confer an additional risk for development of carotid atherosclerosis and arterial thrombosis in type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87079.RArWlETfAHloMapBwoNnwVQ6LI4h2ihry_zFcWAGumurU130_provenance.
- NP87080.RAtCqGOQMMVWsTldis_M01de9zQ971j6OcrPHqyQCmgSc130_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." NP87080.RAtCqGOQMMVWsTldis_M01de9zQ971j6OcrPHqyQCmgSc130_provenance.
- NP87082.RAhhXP36Pz-XuRRV39djDfTC1uv55F_jgFCwnBQbwOWB0130_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." NP87082.RAhhXP36Pz-XuRRV39djDfTC1uv55F_jgFCwnBQbwOWB0130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion description "[GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87094.RAofnyCh6odddjidFKKs_FEfvcWZkM5ofIZMQiYcTrSy4130_assertion description "[The aim of the present observational study was to assess the value of the C825T polymorphism of the beta-3 subunit of G proteins (GNB3) as well as of variants in the SLC6A4 gene (5HTTLPR and STin2 VNTR) and DRD2 gene (TaqI A and NcoI) as predictive markers for consistency in headache response to triptans in migraine patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87094.RAofnyCh6odddjidFKKs_FEfvcWZkM5ofIZMQiYcTrSy4130_provenance.
- NP87101.RAmZmD6vljHq-G923EGFs7bHTkwtl6WG3uxWevmbyWrzE130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87101.RAmZmD6vljHq-G923EGFs7bHTkwtl6WG3uxWevmbyWrzE130_provenance.
- NP87103.RAn2pZPeVIHEL_xAhqCRrowQuMQY-PS0HQgR3rqKtQR0k130_assertion description "[Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87103.RAn2pZPeVIHEL_xAhqCRrowQuMQY-PS0HQgR3rqKtQR0k130_provenance.
- NP87109.RAsFPDoIWxj60p_3uU3tx0JvBEQNtE8CA30EUC5bt1Uy8130_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." NP87109.RAsFPDoIWxj60p_3uU3tx0JvBEQNtE8CA30EUC5bt1Uy8130_provenance.
- NP87112.RAs_5d1TPqFxbiBZMGotL5cVZkrGyX81LTN8KamFF80N0130_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." NP87112.RAs_5d1TPqFxbiBZMGotL5cVZkrGyX81LTN8KamFF80N0130_provenance.
- NP87113.RAv7IzZsV5wi4HM5ws90AlvQeKrt2NbEooJo3WPz4AVl8130_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." NP87113.RAv7IzZsV5wi4HM5ws90AlvQeKrt2NbEooJo3WPz4AVl8130_provenance.
- NP87123.RAgyFATlgmKghRKrjQivhAg3_OnzdVShuwdM4WB211_sQ130_assertion description "[Association of gene polymorphisms with chronic kidney disease in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87123.RAgyFATlgmKghRKrjQivhAg3_OnzdVShuwdM4WB211_sQ130_provenance.
- NP87124.RAgvXwdx3FhncjKeqBW2hB_j5emHFnG1MUFena4kI5GbE130_assertion description "[A pilot study on prostate cancer risk and pro-inflammatory genotypes: pathophysiology and therapeutic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87124.RAgvXwdx3FhncjKeqBW2hB_j5emHFnG1MUFena4kI5GbE130_provenance.
- NP87126.RAvHtL0-uPeCh-O8ePNuJ8wCU4Dpo4BwiyPu_m0Ez_g-s130_assertion description "[An approach based on a genome-wide association study reveals candidate loci for narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87126.RAvHtL0-uPeCh-O8ePNuJ8wCU4Dpo4BwiyPu_m0Ez_g-s130_provenance.
- NP87130.RApWK_QlCITKeeLXxHi70PHARGh853qVbtuS_ELHWxIg4130_assertion description "[Common variants conferring risk of schizophrenia: a pathway analysis of GWAS data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87130.RApWK_QlCITKeeLXxHi70PHARGh853qVbtuS_ELHWxIg4130_provenance.
- NP87132.RAnWDqNgzb3MOmwO7BERerq6aQOPs12CEOhthRw_Vw28E130_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." NP87132.RAnWDqNgzb3MOmwO7BERerq6aQOPs12CEOhthRw_Vw28E130_provenance.
- NP87136.RAm2QEYODlF9TVMzKD-LTmJJcqdbg9S4OTphojmyBqUKE130_assertion description "[The aim of this study was to investigate the association of two polymorphisms in ALOX15 and the risk of coronary artery disease (CAD) in a Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87136.RAm2QEYODlF9TVMzKD-LTmJJcqdbg9S4OTphojmyBqUKE130_provenance.
- NP87137.RApoj0tKddt14iV98JI_nIm_iiYey38hTB0NkExJ-sKm4130_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." NP87137.RApoj0tKddt14iV98JI_nIm_iiYey38hTB0NkExJ-sKm4130_provenance.
- NP87147.RAm_HBmAFdsfXk_08aq3aWjKpRSiHM24Q63m5DSQtdPQQ130_assertion description "[Common variants conferring risk of schizophrenia: a pathway analysis of GWAS data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87147.RAm_HBmAFdsfXk_08aq3aWjKpRSiHM24Q63m5DSQtdPQQ130_provenance.
- NP87148.RAiadLzUcJ6pX1rqeNccWUjcWWXbxR5TG-NapdYuHt9QU130_assertion description "[No association of TAP and LMP genetic polymorphism in human brucellosis and its complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87148.RAiadLzUcJ6pX1rqeNccWUjcWWXbxR5TG-NapdYuHt9QU130_provenance.
- NP87151.RAsVO8_8drnn2QRMpFzpyDZeMGkpyEzffwPWdPSza2KFo130_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." NP87151.RAsVO8_8drnn2QRMpFzpyDZeMGkpyEzffwPWdPSza2KFo130_provenance.
- NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_assertion description "[Usher syndrome is more prevalent than has been reported before the genome project era. Early diagnosis of Usher syndrome has important positive implications for childhood safety, educational planning, genetic counseling, and treatment. The results demonstrate that DNA testing for Usher syndrome is feasible and may be a useful addition to newborn hearing screening programs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_provenance.
- NP87158.RAiIUzMiSjpM_4RKFMEa8LRUi4IvTcPsb7UaYC9xMs6pQ130_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." NP87158.RAiIUzMiSjpM_4RKFMEa8LRUi4IvTcPsb7UaYC9xMs6pQ130_provenance.
- NP87163.RAiTLqw-Io5nGOaixQb-joIr8xhgm1y8vDchzSo1d0lVk130_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." NP87163.RAiTLqw-Io5nGOaixQb-joIr8xhgm1y8vDchzSo1d0lVk130_provenance.
- NP87164.RAg065buEpHYETCNdgOC5eCTTgQ164Mi_ynSIP_rd7zJo130_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." NP87164.RAg065buEpHYETCNdgOC5eCTTgQ164Mi_ynSIP_rd7zJo130_provenance.
- NP87170.RAu2eaQrW8yz3cBNQQ-4HD1wVgC6N56bsM1tEGXBIGuC0130_assertion description "[A study of the single nucleotide polymorphism in seven genes (GHR, IGFBP3, IGFR1, IRS1, FMN1, ANXA2, TaGLN) in ethnic Russians and in patients with prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87170.RAu2eaQrW8yz3cBNQQ-4HD1wVgC6N56bsM1tEGXBIGuC0130_provenance.
- NP87172.RArp343wgFvwk2sHC_gW_OkYr3pd0pE-a6f_7_sceKySI130_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." NP87172.RArp343wgFvwk2sHC_gW_OkYr3pd0pE-a6f_7_sceKySI130_provenance.
- NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_assertion description "[The non-TT genotype at GGH T16C was associated with a high risk of liver dysfunction, presumably because the C allele of GGH C16T may reduce the activity of GGH. The time interval before MTX treatment and rheumatoid factor positivity were associated with the efficacy of MTX treatment. The pharmacogenetics of the MTX pathway genes affects the toxicity and efficacy of MTX in Japanese JIA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87173.RAtaDDzyfr4sF1yTH-a08PbQc6MSmSxdxf98nm5BRtS20130_provenance.