| pubmed-article:17764507 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0427623 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C1412099 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0526260 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C1762617 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C0086222 | lld:lifeskim |
| pubmed-article:17764507 | lifeskim:mentions | umls-concept:C1705733 | lld:lifeskim |
| pubmed-article:17764507 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:17764507 | pubmed:dateCreated | 2007-11-26 | lld:pubmed |
| pubmed-article:17764507 | pubmed:abstractText | Binding of CCAAT-binding factor NF-Y (CBF/NF-Y) to a 43-bp repeat unit in the minisatellite region in the 5' region of the ABO gene (CBF/NF-Y enhancer region) plays an important role in regulating the transcription of ABO genes. The common ABO alleles were found to have CBF/NF-Y enhancer regions with specific numbers of 43-bp minisatellite repeats. | lld:pubmed |
| pubmed-article:17764507 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17764507 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17764507 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17764507 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17764507 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17764507 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17764507 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:17764507 | pubmed:issn | 0041-1132 | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:WagnerFranz... | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:BlasczykRaine... | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:SeltsamAxelA | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:Bade-DoedingC... | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:GrügerDaniela... | lld:pubmed |
| pubmed-article:17764507 | pubmed:author | pubmed-author:GuptaChrista... | lld:pubmed |
| pubmed-article:17764507 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17764507 | pubmed:volume | 47 | lld:pubmed |
| pubmed-article:17764507 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17764507 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17764507 | pubmed:pagination | 2330-5 | lld:pubmed |
| pubmed-article:17764507 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:meshHeading | pubmed-meshheading:17764507... | lld:pubmed |
| pubmed-article:17764507 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17764507 | pubmed:articleTitle | Weak blood group B phenotypes may be caused by variations in the CCAAT-binding factor/NF-Y enhancer region of the ABO gene. | lld:pubmed |
| pubmed-article:17764507 | pubmed:affiliation | Institute for Transfusion Medicine, Hannover Medical School, Hannover, Germany. | lld:pubmed |
| pubmed-article:17764507 | pubmed:publicationType | Journal Article | lld:pubmed |
| entrez-gene:28 | entrezgene:pubmed | pubmed-article:17764507 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:17764507 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17764507 | lld:pubmed |
