pubmed-article:19035517 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0376358 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0012655 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0041740 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0023745 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0694768 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0034606 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0441633 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0025939 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
pubmed-article:19035517 | lifeskim:mentions | umls-concept:C1709701 | lld:lifeskim |
pubmed-article:19035517 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:19035517 | pubmed:dateCreated | 2009-1-29 | lld:pubmed |
pubmed-article:19035517 | pubmed:abstractText | Prostate cancer linkage studies have been used to localize rare and presumably highly penetrant cancer susceptibility genes. Underlying genetic heterogeneity, as well as the high sporadic background of the disease, has resulted in many signals that are often not reproducible between research studies. | lld:pubmed |
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pubmed-article:19035517 | pubmed:language | eng | lld:pubmed |
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pubmed-article:19035517 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:19035517 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19035517 | pubmed:month | Mar | lld:pubmed |
pubmed-article:19035517 | pubmed:issn | 1097-0045 | lld:pubmed |
pubmed-article:19035517 | pubmed:author | pubmed-author:WangYunfeiY | lld:pubmed |
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pubmed-article:19035517 | pubmed:author | pubmed-author:WaltersSarahS | lld:pubmed |
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pubmed-article:19035517 | pubmed:author | pubmed-author:RayAnna MAM | lld:pubmed |
pubmed-article:19035517 | pubmed:author | pubmed-author:EllisJaclynJ | lld:pubmed |
pubmed-article:19035517 | pubmed:copyrightInfo | 2008 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:19035517 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19035517 | pubmed:day | 1 | lld:pubmed |
pubmed-article:19035517 | pubmed:volume | 69 | lld:pubmed |
pubmed-article:19035517 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19035517 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19035517 | pubmed:pagination | 385-91 | lld:pubmed |
pubmed-article:19035517 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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pubmed-article:19035517 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19035517 | pubmed:articleTitle | Genome-wide linkage scan for prostate cancer susceptibility from the University of Michigan Prostate Cancer Genetics Project: suggestive evidence for linkage at 16q23. | lld:pubmed |
pubmed-article:19035517 | pubmed:affiliation | Department of Genetics, University of North Carolina, Chapel Hill, USA. | lld:pubmed |
pubmed-article:19035517 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19035517 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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