| pubmed-article:18251999 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C0337704 | lld:lifeskim |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C0752046 | lld:lifeskim |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C0178587 | lld:lifeskim |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C1285573 | lld:lifeskim |
| pubmed-article:18251999 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:18251999 | pubmed:dateCreated | 2008-3-3 | lld:pubmed |
| pubmed-article:18251999 | pubmed:abstractText | Genetic isolates such as the Ashkenazi Jews (AJ) potentially offer advantages in mapping novel loci in whole genome disease association studies. To analyze patterns of genetic variation in AJ, genotypes of 101 healthy individuals were determined using the Affymetrix EAv3 500 K SNP array and compared to 60 CEPH-derived HapMap (CEU) individuals. 435,632 SNPs overlapped and met annotation criteria in the two groups. | lld:pubmed |
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| pubmed-article:18251999 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18251999 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18251999 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18251999 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18251999 | pubmed:issn | 1471-2156 | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:GilJ BJB | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:OffitKennethK | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:BoydJeffJ | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:ClarkAndrew... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:KirchhoffToma... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:NortonLarryL | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:OlshenAdam... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:SatagopanJaya... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:FriedmanEitan... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:EskinEleazarE | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:BorgenPatrick... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:StruewingJeff... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:LeeCatherine... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:EllisNathan... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:KleinRobert... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:GoldBertB | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:VialeAgnesA | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:LohmuellerKir... | lld:pubmed |
| pubmed-article:18251999 | pubmed:author | pubmed-author:LautenbergerJ... | lld:pubmed |
| pubmed-article:18251999 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18251999 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:18251999 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18251999 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18251999 | pubmed:pagination | 14 | lld:pubmed |
| pubmed-article:18251999 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:meshHeading | pubmed-meshheading:18251999... | lld:pubmed |
| pubmed-article:18251999 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18251999 | pubmed:articleTitle | Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping. | lld:pubmed |
| pubmed-article:18251999 | pubmed:affiliation | Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, USA. olshena@mskcc.org | lld:pubmed |
| pubmed-article:18251999 | pubmed:publicationType | Journal Article | lld:pubmed |
