pubmed-article:18344711 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C0015031 | lld:lifeskim |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C0002395 | lld:lifeskim |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C0596545 | lld:lifeskim |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C0086930 | lld:lifeskim |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:18344711 | lifeskim:mentions | umls-concept:C1517512 | lld:lifeskim |
pubmed-article:18344711 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:18344711 | pubmed:dateCreated | 2008-3-17 | lld:pubmed |
pubmed-article:18344711 | pubmed:abstractText | To describe how investigators in a multisite randomized clinical trial addressed scientific and ethical issues involved in creating risk models based on genetic testing for African American participants. | lld:pubmed |
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