| pubmed-article:17267906 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C1334291 | lld:lifeskim |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C0032463 | lld:lifeskim |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C1527405 | lld:lifeskim |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C0015295 | lld:lifeskim |
| pubmed-article:17267906 | lifeskim:mentions | umls-concept:C0332240 | lld:lifeskim |
| pubmed-article:17267906 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:17267906 | pubmed:dateCreated | 2007-2-1 | lld:pubmed |
| pubmed-article:17267906 | pubmed:abstractText | The V617F mutation, which causes the substitution of phenylalanine for valine at position 617 of the Janus kinase (JAK) 2 gene (JAK2), is often present in patients with polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis. However, the molecular basis of these myeloproliferative disorders in patients without the V617F mutation is unclear. | lld:pubmed |
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| pubmed-article:17267906 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17267906 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17267906 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:17267906 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:17267906 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17267906 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:17267906 | pubmed:issn | 1533-4406 | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:GillilandD... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:StrattonMicha... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:ScottLinda... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:LodishHarvey... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:WeiTongT | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:WarrenAlan... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:ErberWendy... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:GreenAnthony... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:FutrealP... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:ScottMike AMA | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:HarrisonClair... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:McMullinMary... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:LevineRoss... | lld:pubmed |
| pubmed-article:17267906 | pubmed:author | pubmed-author:BeerPhilip... | lld:pubmed |
| pubmed-article:17267906 | pubmed:copyrightInfo | 2007 Massachusetts Medical Society | lld:pubmed |
| pubmed-article:17267906 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17267906 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:17267906 | pubmed:volume | 356 | lld:pubmed |
| pubmed-article:17267906 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17267906 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17267906 | pubmed:pagination | 459-68 | lld:pubmed |
| pubmed-article:17267906 | pubmed:dateRevised | 2010-9-15 | lld:pubmed |
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| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
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| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:meshHeading | pubmed-meshheading:17267906... | lld:pubmed |
| pubmed-article:17267906 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17267906 | pubmed:articleTitle | JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. | lld:pubmed |
| pubmed-article:17267906 | pubmed:affiliation | University of Cambridge, Cambridge, United Kingdom. | lld:pubmed |
