pubmed-article:2430647 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0596227 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0205145 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0019025 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0376315 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0178499 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0205171 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0205117 | lld:lifeskim |
pubmed-article:2430647 | lifeskim:mentions | umls-concept:C0000697 | lld:lifeskim |
pubmed-article:2430647 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:2430647 | pubmed:dateCreated | 1987-1-7 | lld:pubmed |
pubmed-article:2430647 | pubmed:abstractText | The G gamma and A gamma genes of an individual homozygous for the British form of A gamma nondeletion hereditary persistence of fetal hemoglobin have been cloned and partially sequenced. The G gamma gene was normal, but the A gamma gene was found to have a single base change (T----C) at -198 bp relative to the cap site. Supercoiled plasmids containing normal gamma-genes or the mutant A gamma-gene displayed an S1-hypersensitive site immediately 5' to the base change. | lld:pubmed |
pubmed-article:2430647 | pubmed:language | eng | lld:pubmed |
pubmed-article:2430647 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2430647 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:2430647 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2430647 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2430647 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:2430647 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2430647 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2430647 | pubmed:month | Dec | lld:pubmed |
pubmed-article:2430647 | pubmed:issn | 0006-4971 | lld:pubmed |
pubmed-article:2430647 | pubmed:author | pubmed-author:WoodW GWG | lld:pubmed |
pubmed-article:2430647 | pubmed:author | pubmed-author:WeatherallD... | lld:pubmed |
pubmed-article:2430647 | pubmed:author | pubmed-author:TateV EVE | lld:pubmed |
pubmed-article:2430647 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2430647 | pubmed:volume | 68 | lld:pubmed |
pubmed-article:2430647 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2430647 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2430647 | pubmed:pagination | 1389-93 | lld:pubmed |
pubmed-article:2430647 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:meshHeading | pubmed-meshheading:2430647-... | lld:pubmed |
pubmed-article:2430647 | pubmed:year | 1986 | lld:pubmed |
pubmed-article:2430647 | pubmed:articleTitle | The British form of hereditary persistence of fetal hemoglobin results from a single base mutation adjacent to an S1 hypersensitive site 5' to the A gamma globin gene. | lld:pubmed |
pubmed-article:2430647 | pubmed:publicationType | Journal Article | lld:pubmed |
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