| scholarly article | Q13442814 |
| P356 | DOI | 10.4061/2010/790539 |
| P953 | full work available at URL | http://downloads.hindawi.com/journals/ijhy/2010/790539.pdf |
| https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20981302/?tool=EBI | ||
| https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20981302/pdf/?tool=EBI | ||
| http://downloads.hindawi.com/journals/ijhy/2010/790539.xml | ||
| https://europepmc.org/articles/PMC2958466 | ||
| https://europepmc.org/articles/PMC2958466?pdf=render | ||
| P932 | PMC publication ID | 2958466 |
| P698 | PubMed publication ID | 20981302 |
| P5875 | ResearchGate publication ID | 47567247 |
| P2093 | author name string | Ryozo Nagai | |
| Hiroyuki Morita | |||
| Yasushi Imai | |||
| Naomi Ogawa | |||
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| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | genome-wide association study | Q1098876 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | coronary artery disease | Q844935 |
| genome-wide association study | Q1098876 | ||
| P304 | page(s) | 790539 | |
| P577 | publication date | 2010-09-21 | |
| P1433 | published in | International Journal of Hypertension | Q24031588 |
| P1476 | title | Genome-wide association study of coronary artery disease | |
| Genome-Wide Association Study of Coronary Artery Disease | |||
| P478 | volume | 2010 |
| Q39455414 | "Desert" gene (Chr9p21) variants as novel markers for coronary artery disease |
| Q50880534 | A molecular case-control study of association of HNF1A gene polymorphisms (rs2259816 and rs7310409) with risk of coronary artery disease in Iranian patients. |
| Q36279117 | Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients |
| Q47116522 | High expression of long chain acyl-coenzyme A synthetase 1 in peripheral blood may be a molecular marker for assessing the risk of acute myocardial infarction |
| Q35784769 | The effect of hepatic lipase on coronary artery disease in humans is influenced by the underlying lipoprotein phenotype |
| Q36225325 | The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients |
| Q31130783 | Variation in the sodium-dependent vitamin C transporter 2 gene is associated with risk of acute coronary syndrome among women |
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