| pubmed-article:17595049 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C0017296 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C0335038 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C0032136 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C0205102 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C1337112 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:17595049 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
| pubmed-article:17595049 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:17595049 | pubmed:dateCreated | 2007-7-31 | lld:pubmed |
| pubmed-article:17595049 | pubmed:abstractText | Plasmid DNA vectors offer the potential of safe gene therapy avoiding viral vector-mediated toxicity and immunogenicity. As plasmid DNA is bacterial in origin, presence of bacterial lipopolysaccharide (LPS) or unmethylated CpG dinucleotides may stimulate host innate immunity. | lld:pubmed |
| pubmed-article:17595049 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17595049 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17595049 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17595049 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:17595049 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17595049 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17595049 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:17595049 | pubmed:issn | 1099-498X | lld:pubmed |
| pubmed-article:17595049 | pubmed:author | pubmed-author:KirbyJohn AJA | lld:pubmed |
| pubmed-article:17595049 | pubmed:author | pubmed-author:ShawJames A... | lld:pubmed |
| pubmed-article:17595049 | pubmed:author | pubmed-author:RatanamartJar... | lld:pubmed |
| pubmed-article:17595049 | pubmed:author | pubmed-author:HugginsChrist... | lld:pubmed |
| pubmed-article:17595049 | pubmed:copyrightInfo | Copyright 2007 John Wiley & Sons, Ltd. | lld:pubmed |
| pubmed-article:17595049 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17595049 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:17595049 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17595049 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17595049 | pubmed:pagination | 703-14 | lld:pubmed |
| pubmed-article:17595049 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:17595049 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17595049 | pubmed:articleTitle | In vitro and in vivo evaluation of intrinsic immunogenicity of reporter and insulin gene therapy plasmids. | lld:pubmed |
| pubmed-article:17595049 | pubmed:affiliation | Diabetes Research Group, Institute of Cell and Molecular Biosciences, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne NE2 4HH, UK. | lld:pubmed |
| pubmed-article:17595049 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17595049 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17595049 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17595049 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17595049 | lld:pubmed |
