| pubmed-article:21345189 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21345189 | lifeskim:mentions | umls-concept:C0007452 | lld:lifeskim |
| pubmed-article:21345189 | lifeskim:mentions | umls-concept:C0017428 | lld:lifeskim |
| pubmed-article:21345189 | lifeskim:mentions | umls-concept:C1521970 | lld:lifeskim |
| pubmed-article:21345189 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:21345189 | lifeskim:mentions | umls-concept:C1707513 | lld:lifeskim |
| pubmed-article:21345189 | pubmed:dateCreated | 2011-3-11 | lld:pubmed |
| pubmed-article:21345189 | pubmed:abstractText | Copy number variation (CNV) represents another important source of genetic variation complementary to single nucleotide polymorphism (SNP). High-density SNP array data have been routinely used to detect human CNVs, many of which have significant functional effects on gene expression and human diseases. In the dairy industry, a large quantity of SNP genotyping results are becoming available and can be used for CNV discovery to understand and accelerate genetic improvement for complex traits. | lld:pubmed |
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| pubmed-article:21345189 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21345189 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21345189 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21345189 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21345189 | pubmed:issn | 1471-2164 | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:VenturaMarioM | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:SonstegardTad... | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:VEGAYY | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:CardoneMaria... | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:SongJiuzhouJ | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:HouYaliY | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:MatukumalliLa... | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:Van... | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:LiuGeorge EGE | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:BickhartDerek... | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:KimEui-SooES | lld:pubmed |
| pubmed-article:21345189 | pubmed:author | pubmed-author:VanRadenPaul... | lld:pubmed |
| pubmed-article:21345189 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21345189 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:21345189 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21345189 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21345189 | pubmed:pagination | 127 | lld:pubmed |
| pubmed-article:21345189 | pubmed:dateRevised | 2011-7-26 | lld:pubmed |
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| pubmed-article:21345189 | pubmed:meshHeading | pubmed-meshheading:21345189... | lld:pubmed |
| pubmed-article:21345189 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21345189 | pubmed:articleTitle | Genomic characteristics of cattle copy number variations. | lld:pubmed |
| pubmed-article:21345189 | pubmed:affiliation | Bovine Functional Genomics Laboratory, ANRI, USDA-ARS, Beltsville, Maryland 20705, USA. | lld:pubmed |
| pubmed-article:21345189 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21345189 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:21345189 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
