pubmed-article:19505327 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0032105 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0013832 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0441889 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0237753 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0079866 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0015111 | lld:lifeskim |
pubmed-article:19505327 | lifeskim:mentions | umls-concept:C0205349 | lld:lifeskim |
pubmed-article:19505327 | pubmed:dateCreated | 2009-6-18 | lld:pubmed |
pubmed-article:19505327 | pubmed:abstractText | Clinical chemical blood analysis including plasma electrolytes is routinely carried out for the diagnosis of various organ diseases. Phenotype-driven N-ethyl-N-nitrosourea (ENU) mouse mutagenesis projects used plasma electrolytes as parameters for the generation of novel animal models for human diseases. | lld:pubmed |
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pubmed-article:19505327 | pubmed:language | eng | lld:pubmed |
pubmed-article:19505327 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19505327 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19505327 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:19505327 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19505327 | pubmed:issn | 1423-0127 | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:WolfEckhardE | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:AignerBernhar... | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:de... | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:KlemptMartina... | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:RathkolbBirgi... | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:WagnerSibylle... | lld:pubmed |
pubmed-article:19505327 | pubmed:author | pubmed-author:MichelDianD | lld:pubmed |
pubmed-article:19505327 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19505327 | pubmed:volume | 16 | lld:pubmed |
pubmed-article:19505327 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19505327 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19505327 | pubmed:pagination | 53 | lld:pubmed |
pubmed-article:19505327 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:19505327 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19505327 | pubmed:articleTitle | N-ethyl-N-nitrosourea mutagenesis produced a small number of mice with altered plasma electrolyte levels. | lld:pubmed |
pubmed-article:19505327 | pubmed:affiliation | Chair for Molecular Animal Breeding and Biotechnology, Department of Veterinary Sciences, and Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, LMU Munich, Munich, Germany. b.aigner@gen.vetmed.uni-muenchen.de | lld:pubmed |
pubmed-article:19505327 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19505327 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |