pubmed-article:20454657 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C1257890 | lld:lifeskim |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C0237753 | lld:lifeskim |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C0392756 | lld:lifeskim |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C0018591 | lld:lifeskim |
pubmed-article:20454657 | lifeskim:mentions | umls-concept:C1880371 | lld:lifeskim |
pubmed-article:20454657 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:20454657 | pubmed:dateCreated | 2010-5-10 | lld:pubmed |
pubmed-article:20454657 | pubmed:abstractText | The high levels of variation characterising the mitochondrial DNA (mtDNA) molecule are due ultimately to its high average mutation rate; moreover, mtDNA variation is deeply structured in different populations and ethnic groups. There is growing interest in selecting a reduced number of mtDNA single nucleotide polymorphisms (mtSNPs) that account for the maximum level of discrimination power in a given population. Applications of the selected mtSNP panel range from anthropologic and medical studies to forensic genetic casework. | lld:pubmed |
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pubmed-article:20454657 | pubmed:language | eng | lld:pubmed |
pubmed-article:20454657 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20454657 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20454657 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20454657 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20454657 | pubmed:issn | 1932-6203 | lld:pubmed |
pubmed-article:20454657 | pubmed:author | pubmed-author:SalasAntonioA | lld:pubmed |
pubmed-article:20454657 | pubmed:author | pubmed-author:AmigoJorgeJ | lld:pubmed |
pubmed-article:20454657 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20454657 | pubmed:volume | 5 | lld:pubmed |
pubmed-article:20454657 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20454657 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20454657 | pubmed:pagination | e10218 | lld:pubmed |
pubmed-article:20454657 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
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pubmed-article:20454657 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20454657 | pubmed:articleTitle | A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups. | lld:pubmed |
pubmed-article:20454657 | pubmed:affiliation | Unidade de Xenética, Departamento de Anatomía Patolóxica e Ciencias Forenses, Universidade de Santiago de Compostela, Galicia, Spain. antonio.salas@usc.es | lld:pubmed |
pubmed-article:20454657 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20454657 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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