pubmed-article:18213635 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C1516213 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C0376358 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C1515464 | lld:lifeskim |
pubmed-article:18213635 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
pubmed-article:18213635 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:18213635 | pubmed:dateCreated | 2008-2-28 | lld:pubmed |
pubmed-article:18213635 | pubmed:abstractText | Multiple variants in three regions at 8q24 are consistently found to be associated with prostate cancer (PCa) risk in population-based association studies. The role that these variants may play in familial prostate cancer risk has not been extensively investigated. | lld:pubmed |
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pubmed-article:18213635 | pubmed:language | eng | lld:pubmed |
pubmed-article:18213635 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18213635 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18213635 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18213635 | pubmed:month | Apr | lld:pubmed |
pubmed-article:18213635 | pubmed:issn | 0270-4137 | lld:pubmed |
pubmed-article:18213635 | pubmed:author | pubmed-author:XuJianfengJ | lld:pubmed |
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pubmed-article:18213635 | pubmed:author | pubmed-author:ChangBao-LiBL | lld:pubmed |
pubmed-article:18213635 | pubmed:author | pubmed-author:DugganDavidD | lld:pubmed |
pubmed-article:18213635 | pubmed:author | pubmed-author:LangeLeslieL | lld:pubmed |
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pubmed-article:18213635 | pubmed:author | pubmed-author:SunJielinJ | lld:pubmed |
pubmed-article:18213635 | pubmed:author | pubmed-author:LiuWennuanW | lld:pubmed |
pubmed-article:18213635 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18213635 | pubmed:day | 1 | lld:pubmed |
pubmed-article:18213635 | pubmed:volume | 68 | lld:pubmed |
pubmed-article:18213635 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18213635 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18213635 | pubmed:pagination | 489-97 | lld:pubmed |
pubmed-article:18213635 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:18213635 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18213635 | pubmed:articleTitle | Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients. | lld:pubmed |
pubmed-article:18213635 | pubmed:affiliation | Center for Human Genomics, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA. | lld:pubmed |
pubmed-article:18213635 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18213635 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:18213635 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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