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Volumn 55, Issue 3, 2009, Pages

Ontology driven modeling for the knowledge of genetic susceptibility to disease

Author keywords

Genetic susceptibility; Knowledge representation; Modeling; Ontology; OWL

Indexed keywords

ARTICLE; BIOMEDICINE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HEREDITY;

EID: 75749089722     PISSN: 00232513     EISSN: 18830498     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (24)
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    • Ontologies in bioinformatics and systems biology
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    • Lambrix, P.1
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    • Smith, B., Ashburner, M., Rosse, C., Bard, J., Bug, W., Ceusters, W., Goldberg, L. J., Eilbeck, K., Ireland, A., Mungall, C. J., The OBI Consortium, Leontis, N., Rocca-Serra, P., Ruttenberg, A., Sansone, S., Scheuermann, R. H., Shah, N., Whetzel, P. L., Lewis, S. 2007.The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration. Nat. Biotechnol. 25:1251-1255.
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    • A Common Polymorphism in the Upstream Promoter Region of the Hepatocyte Nuclear Factor-4 Gene on Chromosome 20q Is Associated With Type 2 Diabetes and Appears to Contribute to the Evidence for Linkage in an Ashkenazi Jewish Population
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    • Love-Gregory, L. D., Wasson J., Ma J., Jin C. H., Glaser B., Suarez, B. K. and Permutt, M. A. 2004. A Common Polymorphism in the Upstream Promoter Region of the Hepatocyte Nuclear Factor-4 Gene on Chromosome 20q Is Associated With Type 2 Diabetes and Appears to Contribute to the Evidence for Linkage in an Ashkenazi Jewish Population. Diabetes Apr, p.1134-1140.
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    • Love-Gregory, L.D.1    Wasson, J.2    Ma, J.3    Jin, C.H.4    Glaser, B.5    Suarez, B.K.6    Permutt, M.A.7
  • 16
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    • Genome-wide Association Studies: Theoretical and practical concerns
    • Wang, W. Y. S., Barratt, B. J., Clayton, D. G. and Todd, J.A. 2005. Genome-wide Association Studies: theoretical and practical concerns. Nat Rev Genet. 6(2):109-18.
    • (2005) Nat Rev Genet , vol.6 , Issue.2 , pp. 109-118
    • Wang, W.Y.S.1    Barratt, B.J.2    Clayton, D.G.3    Todd, J.A.4
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    • Single Nucleotide Transcription factor 7-like 2 (TCF7L2) Gene Polymorphisms in Anti-Islet Autoantibody Negative Patients at Onset of Diabetes
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    • Yu J, Steck, A.K., Babu, S., Yu, L., Miao, D., McFann, K., Hutton, J., Eisenbarth, G.S., Klingensmith, G. 2008 Single Nucleotide Transcription factor 7-like 2 (TCF7L2) Gene Polymorphisms in Anti-Islet Autoantibody Negative Patients at Onset of Diabetes. J Clin Endocrinol Metab. doi: 10.1210/jc.2007-2694
    • (2008) J Clin Endocrinol Metab
    • Yu, J.1    Steck, A.K.2    Babu, S.3    Yu, L.4    Miao, D.5    McFann, K.6    Hutton, J.7    Eisenbarth, G.S.8    Klingensmith, G.9
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    • Marquezine, G.F., Pereira, A.C., Sousa, A.G., Mill, J.G., Hueb, W.A., Krieger, J.E. 2008. TCF7L2 variant genotypes and type 2 diabetes risk in Brazil: significant association, but not a significant tool for risk stratification in the general population. BMC Med Genet. 9(1):106.
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    • Marquezine, G.F.1    Pereira, A.C.2    Sousa, A.G.3    Mill, J.G.4    Hueb, W.A.5    Krieger, J.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.