Nanopublications

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

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NP93478.RAs33yeTJSh-tvbr31SpJMdONmyaRjMNh-ge5qmNNNi3c130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93478.RAs33yeTJSh-tvbr31SpJMdONmyaRjMNh-ge5qmNNNi3c130_provenance.
NP93486.RAovu2NwhRZzzURHRc7MbA7J7SqhmGdkx6rqU1nzqw7wI130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93486.RAovu2NwhRZzzURHRc7MbA7J7SqhmGdkx6rqU1nzqw7wI130_provenance.
NP93494.RAgYeOqg6gmODzjfokbSt2376AkWZUOYMb8Bqmk68xIaE130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93494.RAgYeOqg6gmODzjfokbSt2376AkWZUOYMb8Bqmk68xIaE130_provenance.
NP93498.RAvlh_hYg0hEOwVAMdhpotZp8-BPCTPA6vDFbaFCH4RWc130_assertion description "[We generated publicly available genotype data for sporadic ALS patients and controls. No single locus was definitively associated with increased risk of developing disease, although potentially associated candidate SNPs were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93498.RAvlh_hYg0hEOwVAMdhpotZp8-BPCTPA6vDFbaFCH4RWc130_provenance.
NP93504.RAhintkKODagVkSDgXWb3sN3JnqTFwWlA_zWIuzE8SW5Q130_assertion description "[Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93504.RAhintkKODagVkSDgXWb3sN3JnqTFwWlA_zWIuzE8SW5Q130_provenance.
NP93518.RAjPZg3C2wxwuz1jjmGXtjsddcMz7lXyDQVdFg9QwuPWk130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93518.RAjPZg3C2wxwuz1jjmGXtjsddcMz7lXyDQVdFg9QwuPWk130_provenance.
NP93520.RAjK5VIAuQxo97OMPUrH4840yGWSwjxz74cm6HrITkO54130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93520.RAjK5VIAuQxo97OMPUrH4840yGWSwjxz74cm6HrITkO54130_provenance.
NP93528.RAiaihCY6_WbqIUy40P8rSC9YuHMjPPudWiQcecCvIDVs130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93528.RAiaihCY6_WbqIUy40P8rSC9YuHMjPPudWiQcecCvIDVs130_provenance.
NP93532.RAmYfrBxDkRgiR_ZxbuzB88AdmsRJYE0_uyaUtWsX0fW0130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93532.RAmYfrBxDkRgiR_ZxbuzB88AdmsRJYE0_uyaUtWsX0fW0130_provenance.
NP93535.RAoYoVsLUawU9Lfm0LJE1z63dc7z7ws0ntJjiTzPYERVw130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93535.RAoYoVsLUawU9Lfm0LJE1z63dc7z7ws0ntJjiTzPYERVw130_provenance.
NP93536.RAmZ1LV_D5pXi3O_kD9Nsp1xmqtGSu0jgoYPWaSs_4b00130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93536.RAmZ1LV_D5pXi3O_kD9Nsp1xmqtGSu0jgoYPWaSs_4b00130_provenance.
NP93537.RAuIFo1z6b-osJMbc4oUl6rY5DelyunaYtVinZRnEZQeM130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93537.RAuIFo1z6b-osJMbc4oUl6rY5DelyunaYtVinZRnEZQeM130_provenance.
NP93545.RAmxi4MiUyTdexz6pb7cbKbt5VFp8U0lxp3VCQpDwavhE130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93545.RAmxi4MiUyTdexz6pb7cbKbt5VFp8U0lxp3VCQpDwavhE130_provenance.
NP93546.RAmBXONJK2OWBptMhHVTIMubKzyWcNQvH3oS47X-kfgAU130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93546.RAmBXONJK2OWBptMhHVTIMubKzyWcNQvH3oS47X-kfgAU130_provenance.
NP93554.RAgsNzgtM0PQbTgzcZBvDU27b51sSM1X1BwQssgW7w11c130_assertion description "[The data generated here comprise the first phase of a genome-wide association analysis in patients with stroke. Release of phase I results generated in these publicly available samples from each consenting individual makes this dataset a valuable resource for data-mining and augmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93554.RAgsNzgtM0PQbTgzcZBvDU27b51sSM1X1BwQssgW7w11c130_provenance.
NP93557.RAl3_vPq3axxGWnFDrl4mHGSjhKd952AoKUa8tLiY5x4A130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93557.RAl3_vPq3axxGWnFDrl4mHGSjhKd952AoKUa8tLiY5x4A130_provenance.
NP93560.RAsC5FAbfn8RlMuNm1KdqtgN9qyPR3BIhH8-TlhScsHmU130_assertion description "[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93560.RAsC5FAbfn8RlMuNm1KdqtgN9qyPR3BIhH8-TlhScsHmU130_provenance.
NP93565.RAqAGZzPfpp3C0LOYflJvT2STQUJbPaWUIZ2aageVMag0130_assertion description "[Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93565.RAqAGZzPfpp3C0LOYflJvT2STQUJbPaWUIZ2aageVMag0130_provenance.
NP93568.RAuQiwAS4bFspvvifZtqJqfMvn29KZV6hBgNc9DVQlGek130_assertion description "[Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93568.RAuQiwAS4bFspvvifZtqJqfMvn29KZV6hBgNc9DVQlGek130_provenance.
NP93569.RAk99L2kgkKmkE6YVJxC3MlpKoejkimmoguVR5qMOrRtg130_assertion description "[We observed numerous regions with suggestive associations with type 2 diabetes. Some of these signals correspond to regions described in previous studies. However, many of these regions could not be replicated in the DIAGRAM datasets. It is critical to carry out additional studies in Hispanic and American Indian populations, which have a high prevalence of type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93569.RAk99L2kgkKmkE6YVJxC3MlpKoejkimmoguVR5qMOrRtg130_provenance.
NP93570.RAiDiuTXNp-5E4oX_iqSDdaJJV2reQB63sjBtV9Mq3pEA130_assertion description "[1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93570.RAiDiuTXNp-5E4oX_iqSDdaJJV2reQB63sjBtV9Mq3pEA130_provenance.
NP93572.RAmyRcGCP0Y5wg9Dev9-whO5WqGBotE4T42ZneWkUZXWg130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93572.RAmyRcGCP0Y5wg9Dev9-whO5WqGBotE4T42ZneWkUZXWg130_provenance.
NP93573.RAh1xPOjztDfPJWSdgueyV5Na8l8bX0O8jz8lWDwcoE3s130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93573.RAh1xPOjztDfPJWSdgueyV5Na8l8bX0O8jz8lWDwcoE3s130_provenance.
NP93585.RAtD9VvtbYM7uKWTECFce6ey9iE9WfYeVNfDYlQquJUH4130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93585.RAtD9VvtbYM7uKWTECFce6ey9iE9WfYeVNfDYlQquJUH4130_provenance.
NP93586.RArmsV2rG5TCMCAaVVmMZTNDgEp-V0PK3u4-VvgjjAMc0130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93586.RArmsV2rG5TCMCAaVVmMZTNDgEp-V0PK3u4-VvgjjAMc0130_provenance.
NP93589.RAnWEmFhuY4GgGw5PmM_jaSP4rNnBXjRSXPcD7iPSGq74130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93589.RAnWEmFhuY4GgGw5PmM_jaSP4rNnBXjRSXPcD7iPSGq74130_provenance.
NP93590.RAvpF7aCPxgbCKwms2xfn82LsyjH5DHzan2Iw4qwA6yrs130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93590.RAvpF7aCPxgbCKwms2xfn82LsyjH5DHzan2Iw4qwA6yrs130_provenance.
NP93601.RArWJPSIqhd8a8YTK84Ir0HUAf87mho1zB0cZHQJHV2AI130_assertion description "[A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93601.RArWJPSIqhd8a8YTK84Ir0HUAf87mho1zB0cZHQJHV2AI130_provenance.
NP93610.RAg8XcUDuGgQ-Ji9HrG-nIXJ_vsulQzx3pRF8dr-4-bcc130_assertion description "[Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93610.RAg8XcUDuGgQ-Ji9HrG-nIXJ_vsulQzx3pRF8dr-4-bcc130_provenance.
NP93614.RAiNL-Jki_rK1e_5f9CDEw_4Zs2C-71Og2J_FpSWFqINA130_assertion description "[Type 1 diabetes (T1D) in children results from autoimmune destruction of pancreatic beta cells, leading to insufficient production of insulin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93614.RAiNL-Jki_rK1e_5f9CDEw_4Zs2C-71Og2J_FpSWFqINA130_provenance.
NP93616.RAp6abLdbNtRplRgjIO1OmMvreE216E-D7F55t3BAVr0I130_assertion description "[Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93616.RAp6abLdbNtRplRgjIO1OmMvreE216E-D7F55t3BAVr0I130_provenance.
NP93619.RAicLRLK1uiWDvjFx_rYNNEFaYc9VLdh6pTRW1oaHYkUk130_assertion description "[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93619.RAicLRLK1uiWDvjFx_rYNNEFaYc9VLdh6pTRW1oaHYkUk130_provenance.
NP93621.RAmUBkpBbPhS-h8CWvDFEOndCqxCT_OktYt6NfxN2tEMw130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93621.RAmUBkpBbPhS-h8CWvDFEOndCqxCT_OktYt6NfxN2tEMw130_provenance.
NP93626.RAvPvtotyz8tJTomwknSFlxhnU9oyrg0VD2GRvtaaIPXc130_assertion description "[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93626.RAvPvtotyz8tJTomwknSFlxhnU9oyrg0VD2GRvtaaIPXc130_provenance.
NP93639.RAjOGawf8fgLUXGx8AiiKgJ_VAxxL_Gq9fMCci--l-elM130_assertion description "[We identified several genetic loci that, individually and in aggregate, substantially affect the risk of development of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93639.RAjOGawf8fgLUXGx8AiiKgJ_VAxxL_Gq9fMCci--l-elM130_provenance.
NP93640.RAhcM05tccUnwXVfHCE3Q0wQEWwuFDfMx6BynS8hiBcTo130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93640.RAhcM05tccUnwXVfHCE3Q0wQEWwuFDfMx6BynS8hiBcTo130_provenance.
NP93652.RAiVXuCw2m87pvvHVdxxm2snrN1vR1W9fIEQXMie8cj4Q130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93652.RAiVXuCw2m87pvvHVdxxm2snrN1vR1W9fIEQXMie8cj4Q130_provenance.
NP93654.RAh6SGi4z464sJ_vOgfAV9ReUAouGSRp6aNIOb73qJpxE130_assertion description "[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93654.RAh6SGi4z464sJ_vOgfAV9ReUAouGSRp6aNIOb73qJpxE130_provenance.
NP93659.RAsPuqK-RgAD72voEyUKeCQnjlV1S0k0D9-Hr0O9uITDk130_assertion description "[Multiple loci identified in a genome-wide association study of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93659.RAsPuqK-RgAD72voEyUKeCQnjlV1S0k0D9-Hr0O9uITDk130_provenance.
NP93672.RAoV58ch2V0z20ELYqDzxEd5XYuLwFRWkYjr9gVA_eyXI130_assertion description "[Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93672.RAoV58ch2V0z20ELYqDzxEd5XYuLwFRWkYjr9gVA_eyXI130_provenance.
NP93679.RAinot3eA-8iBht0EndBFhXmcWvnRnP_y94NYczW1ClAo130_assertion description "[Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93679.RAinot3eA-8iBht0EndBFhXmcWvnRnP_y94NYczW1ClAo130_provenance.
NP93681.RAhY7mA_2_Uvar-2Uxn0ehg8B-t8uikSA5Hy1srBdPnVE130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93681.RAhY7mA_2_Uvar-2Uxn0ehg8B-t8uikSA5Hy1srBdPnVE130_provenance.
NP93687.RArMKKDF5Mr2Lwq0u1fG_EnYtWHi8yJCOGYT7RllyaJPo130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93687.RArMKKDF5Mr2Lwq0u1fG_EnYtWHi8yJCOGYT7RllyaJPo130_provenance.
NP93692.RAlHQj49gi6z0Ic8ofrGNgJUUNVSf6COJU1f02gn01ABg130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93692.RAlHQj49gi6z0Ic8ofrGNgJUUNVSf6COJU1f02gn01ABg130_provenance.
NP93695.RAm0ihR64ZU-vIWXozOnybSu-jRy88Uo7_pYtL2IBaE_U130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93695.RAm0ihR64ZU-vIWXozOnybSu-jRy88Uo7_pYtL2IBaE_U130_provenance.
NP93696.RAmNIw9GUxFwthWjiGJDitEWPgpIVZ-zmu-5KQu_SVG0o130_assertion description "[Alleles of IL2RA and IL7RA and those in the HLA locus are identified as heritable risk factors for multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93696.RAmNIw9GUxFwthWjiGJDitEWPgpIVZ-zmu-5KQu_SVG0o130_provenance.
NP93708.RAhjabSTLFlqZEwHo_xenrFwGrlJVIywMs_ha5iK-7K74130_assertion description "[We were able to replicate association of one SNP within the PDE4D gene in a second sample collected by our laboratory and in a family-based test in an independent sample; however, the SNP was not significantly associated with neuroticism in two other independent samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93708.RAhjabSTLFlqZEwHo_xenrFwGrlJVIywMs_ha5iK-7K74130_provenance.
NP93709.RAgoPC9lCfzb3hdFZStEGqeA0Cp-ebWhJKpVLGrd2i5-A130_assertion description "[Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93709.RAgoPC9lCfzb3hdFZStEGqeA0Cp-ebWhJKpVLGrd2i5-A130_provenance.
NP93714.RAnN2ZrKy1xrH6bbAsfyrKFy0ywGQb3YIblAQuUU-_Sps130_assertion description "[Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93714.RAnN2ZrKy1xrH6bbAsfyrKFy0ywGQb3YIblAQuUU-_Sps130_provenance.
NP93718.RAquWscW8U61Fk98AeGxq-fvtCO85pa6CdsUWmUA3zOuU130_assertion description "[Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93718.RAquWscW8U61Fk98AeGxq-fvtCO85pa6CdsUWmUA3zOuU130_provenance.
NP93720.RArqHutolswal7jY9U-hnQcOT4ZCh_24jHAzsfWHzxfJg130_assertion description "[Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93720.RArqHutolswal7jY9U-hnQcOT4ZCh_24jHAzsfWHzxfJg130_provenance.
NP93721.RAiQX9yPv1zfqbq6i1TG5hKo2iSfD2GsjpgHPxc0Ai4Ko130_assertion description "[Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93721.RAiQX9yPv1zfqbq6i1TG5hKo2iSfD2GsjpgHPxc0Ai4Ko130_provenance.
NP93723.RAurjhdzshLKg1qoQTmvRX_Q5mJs-RagvVDunVHFYoOp4130_assertion description "[Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93723.RAurjhdzshLKg1qoQTmvRX_Q5mJs-RagvVDunVHFYoOp4130_provenance.
NP93738.RAgYF3kOP6Zf1DSoGBZca7CpNG6CjT4Eql0719a6GUS6k130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93738.RAgYF3kOP6Zf1DSoGBZca7CpNG6CjT4Eql0719a6GUS6k130_provenance.
NP93744.RAmvuQuMWDpCP3bxRzeU8gH2vGYVwS6ogLtivXzp5TF0E130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93744.RAmvuQuMWDpCP3bxRzeU8gH2vGYVwS6ogLtivXzp5TF0E130_provenance.
NP93746.RAqW_7piKUAra0QTtLlSM638OaJv3_gYnh4A5tkeYmPLA130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93746.RAqW_7piKUAra0QTtLlSM638OaJv3_gYnh4A5tkeYmPLA130_provenance.
NP93755.RAhOyJ7Nt4QeHfW54XiqSVDlXn5JbFIZ44yQblvGR0vmM130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93755.RAhOyJ7Nt4QeHfW54XiqSVDlXn5JbFIZ44yQblvGR0vmM130_provenance.
NP93756.RAnuuxvjhqUbecejVmgkosMowFj3xZmIDHiX-xTYcNhmM130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93756.RAnuuxvjhqUbecejVmgkosMowFj3xZmIDHiX-xTYcNhmM130_provenance.
NP93760.RAi3_ittr0JwdhCPLma2nt_2G8Hhijgx8ytKaoiAb8uF8130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93760.RAi3_ittr0JwdhCPLma2nt_2G8Hhijgx8ytKaoiAb8uF8130_provenance.
NP93762.RAoiQa7b_XbJrbML2rhkvNuF4Mpc1lu0fXiG8r7ESHYTM130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93762.RAoiQa7b_XbJrbML2rhkvNuF4Mpc1lu0fXiG8r7ESHYTM130_provenance.
NP93763.RApPvas4IphOEk0fTJt7h5SWY4qhD-af3sgvdt1oOS89Q130_assertion description "[Longevity and aging traits are associated with SNPs on the Affymetrix 100K GeneChip. None of the associations achieved genome-wide significance. These data generate hypotheses and serve as a resource for replication as more genes and biologic pathways are proposed as contributing to longevity and healthy aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93763.RApPvas4IphOEk0fTJt7h5SWY4qhD-af3sgvdt1oOS89Q130_provenance.
NP93764.RAimbaTM-3nVG_pX2UFC4ZYDRjHMdKUgofBDPjpf9O3H8130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93764.RAimbaTM-3nVG_pX2UFC4ZYDRjHMdKUgofBDPjpf9O3H8130_provenance.
NP93765.RAm6PvhsvSoQX0jnY0N7TYb7QziWwm3e8CoPJsr6J6PkM130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93765.RAm6PvhsvSoQX0jnY0N7TYb7QziWwm3e8CoPJsr6J6PkM130_provenance.
NP93769.RAmFwz75cGQ839f_pcGdew70HXEdxdRQ83w8NC3W8HjIQ130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93769.RAmFwz75cGQ839f_pcGdew70HXEdxdRQ83w8NC3W8HjIQ130_provenance.
NP93772.RAo8FAIVp9ZTwbkr-qTPsaXQtTtFoLBQ0wMKJ3iXaMVJU130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93772.RAo8FAIVp9ZTwbkr-qTPsaXQtTtFoLBQ0wMKJ3iXaMVJU130_provenance.
NP93776.RAlTfro4bfRkE8AFGNzEubkFXCUW_-70CYrqBFC1OPpJA130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93776.RAlTfro4bfRkE8AFGNzEubkFXCUW_-70CYrqBFC1OPpJA130_provenance.
NP93781.RAhIaLRg0aoAlhJdbpcNuqSmAp_724a8qTkZF_G22oGmo130_assertion description "[The FHS 100K SNP project offers an unbiased genome-wide strategy to identify new candidate loci and to replicate previously suggested candidate genes for osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93781.RAhIaLRg0aoAlhJdbpcNuqSmAp_724a8qTkZF_G22oGmo130_provenance.
NP93785.RAtZI06a26XXW7FdE5owHD5yqB-Yr9EMObPHj3HPacd_M130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93785.RAtZI06a26XXW7FdE5owHD5yqB-Yr9EMObPHj3HPacd_M130_provenance.
NP93792.RAmLvR466bu54LTAB0mGm1GYVqyIncx3e_zn6m_8Fldns130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93792.RAmLvR466bu54LTAB0mGm1GYVqyIncx3e_zn6m_8Fldns130_provenance.
NP93794.RAguuOgMsQbRpnIlscZMbjbtk1xyrLcCd2YVdk5GpUqKQ130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93794.RAguuOgMsQbRpnIlscZMbjbtk1xyrLcCd2YVdk5GpUqKQ130_provenance.
NP93802.RAjzR4aEac5zZ-Og77SearcCelWzCzTtRxtC1sYMkNIqI130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93802.RAjzR4aEac5zZ-Og77SearcCelWzCzTtRxtC1sYMkNIqI130_provenance.
NP93803.RAiQH2dmpKhv8Zm-YGMA6q2xZ3TA8gH4WXNEKT3SyD7Zw130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93803.RAiQH2dmpKhv8Zm-YGMA6q2xZ3TA8gH4WXNEKT3SyD7Zw130_provenance.
NP93810.RAqKSM11Pb2x4ZeycIimEVmQStxAmulsBFtsub4nWI8vY130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93810.RAqKSM11Pb2x4ZeycIimEVmQStxAmulsBFtsub4nWI8vY130_provenance.
NP93815.RAkMFLfK-g4ho3cY5vRgzLg7-3dtVBxg_iJz1XotDZE-I130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93815.RAkMFLfK-g4ho3cY5vRgzLg7-3dtVBxg_iJz1XotDZE-I130_provenance.
NP93816.RApfdIhccPJbWTGSFGTVmOhjdFLdaLSFZxgAHwrhoE2vk130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93816.RApfdIhccPJbWTGSFGTVmOhjdFLdaLSFZxgAHwrhoE2vk130_provenance.
NP93818.RAjJmLW-QKhQ6WrdxSOooMgRV0XSwMYMavvJ0w1yRArZw130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93818.RAjJmLW-QKhQ6WrdxSOooMgRV0XSwMYMavvJ0w1yRArZw130_provenance.
NP93821.RAoiidU2tHjUWMVEtT32Awxpw50kKAAKOOCmMLZwGlQnU130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93821.RAoiidU2tHjUWMVEtT32Awxpw50kKAAKOOCmMLZwGlQnU130_provenance.
NP93830.RAmCrWgXESSGV_f5SayVbm6wEBVGXAbdIW6j6aTrysZ9s130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93830.RAmCrWgXESSGV_f5SayVbm6wEBVGXAbdIW6j6aTrysZ9s130_provenance.
NP93831.RAkxA7Ucjqk7N-d38kpp40HfJ-mfs-SMHw69gaCTOna00130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93831.RAkxA7Ucjqk7N-d38kpp40HfJ-mfs-SMHw69gaCTOna00130_provenance.
NP93832.RAoBlK26LPlXeA9KeT5pfKtMfJzp0pCq2BiTTtMxrqS9A130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93832.RAoBlK26LPlXeA9KeT5pfKtMfJzp0pCq2BiTTtMxrqS9A130_provenance.
NP93840.RAqT_5swacvsO86W4iHgXmZLBb2sfNhwDAl9iF92xE6Hc130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93840.RAqT_5swacvsO86W4iHgXmZLBb2sfNhwDAl9iF92xE6Hc130_provenance.
NP93843.RAtSxZSuMi9xOu1D4o7z40Kq1wqVTAWmPz5IW65ZLGDxk130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93843.RAtSxZSuMi9xOu1D4o7z40Kq1wqVTAWmPz5IW65ZLGDxk130_provenance.
NP93846.RAqRrqrR3MEXkB04_ZIYXFUcHI4_OFLo-0MRaJ29DET4A130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93846.RAqRrqrR3MEXkB04_ZIYXFUcHI4_OFLo-0MRaJ29DET4A130_provenance.
NP93854.RAiw4tZYyj1tblKCs7Xy6M0r1bicZJVObatOFL-WGLnIU130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93854.RAiw4tZYyj1tblKCs7Xy6M0r1bicZJVObatOFL-WGLnIU130_provenance.
NP93862.RAqgLLYn2XH9oCYtatNlUS8lgxW3wJseOsg8vBsNBU_Nc130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93862.RAqgLLYn2XH9oCYtatNlUS8lgxW3wJseOsg8vBsNBU_Nc130_provenance.
NP93865.RAsAP4yHE-37oqNIDVVFv6asUWqhGMeC9p469HTrvwuIo130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93865.RAsAP4yHE-37oqNIDVVFv6asUWqhGMeC9p469HTrvwuIo130_provenance.
NP93870.RAuGgyLFbaJ1bMrR6Ac0rXOFuphsiv2rk_bNOO-E7RPW8130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93870.RAuGgyLFbaJ1bMrR6Ac0rXOFuphsiv2rk_bNOO-E7RPW8130_provenance.
NP93873.RArU6eS7_oNUvAcl6lzI4MKD7r4ZLyodxy4Lg2jfbNzOQ130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93873.RArU6eS7_oNUvAcl6lzI4MKD7r4ZLyodxy4Lg2jfbNzOQ130_provenance.
NP93879.RAigm_rwsnrCwZBfkBgmLLh-y1uJO8mS1LP9jBR0ujV6c130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93879.RAigm_rwsnrCwZBfkBgmLLh-y1uJO8mS1LP9jBR0ujV6c130_provenance.
NP93881.RAhqB_wO7bJonwGpAgzyGIbTUjWJ74gEPuCEj7KMER1T4130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93881.RAhqB_wO7bJonwGpAgzyGIbTUjWJ74gEPuCEj7KMER1T4130_provenance.
NP93884.RAnxvLSBiTiXElQ04pYDYhbn_vKmvwyTkPIfyfEvVUZj0130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93884.RAnxvLSBiTiXElQ04pYDYhbn_vKmvwyTkPIfyfEvVUZj0130_provenance.
NP93885.RAusX42VWVyfNn9xxuI1K0CYWzZPJMwXlMvr6M7bLi7fw130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93885.RAusX42VWVyfNn9xxuI1K0CYWzZPJMwXlMvr6M7bLi7fw130_provenance.
NP93888.RAu2TsRzKwrqzDP80WCAT6NRmsV2UFx3_O1Mjt_IsJEtU130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93888.RAu2TsRzKwrqzDP80WCAT6NRmsV2UFx3_O1Mjt_IsJEtU130_provenance.
NP93889.RAt9ZdJmsU0KG8Ln8Wmm0CuXyW8djMn3OgxAxfjIT6JX8130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93889.RAt9ZdJmsU0KG8Ln8Wmm0CuXyW8djMn3OgxAxfjIT6JX8130_provenance.
NP93892.RAmrinNYovjzAoCM3H_PNYBzbhP8AB8B_ocSoXYa53lVY130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93892.RAmrinNYovjzAoCM3H_PNYBzbhP8AB8B_ocSoXYa53lVY130_provenance.
NP93893.RAixN5JHoK9sMqjp6gUV0aQLp_3qpcvVCBEAlna-xv3HY130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93893.RAixN5JHoK9sMqjp6gUV0aQLp_3qpcvVCBEAlna-xv3HY130_provenance.
NP93894.RAob8f_XWflu_kgdglMfy7VSHh0vpePMegiK7sd5f_Mgg130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93894.RAob8f_XWflu_kgdglMfy7VSHh0vpePMegiK7sd5f_Mgg130_provenance.
NP93897.RAiGQpMhJ-0y-UwyUpoPxVADhSV3iHMmO6f2X7GScC-HE130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93897.RAiGQpMhJ-0y-UwyUpoPxVADhSV3iHMmO6f2X7GScC-HE130_provenance.
NP93898.RAhm3Fkiu4huVuPMh_27tIxstqseBJwsucnwmINOKJ-fo130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93898.RAhm3Fkiu4huVuPMh_27tIxstqseBJwsucnwmINOKJ-fo130_provenance.
NP93902.RAuQ3KzGgBrpc502_Fi0derNfAYP2Ki-ZQIgG5tenDwwY130_assertion description "[Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93902.RAuQ3KzGgBrpc502_Fi0derNfAYP2Ki-ZQIgG5tenDwwY130_provenance.

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