pubmed-article:17404368 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17404368 | lifeskim:mentions | umls-concept:C0006142 | lld:lifeskim |
pubmed-article:17404368 | lifeskim:mentions | umls-concept:C1519429 | lld:lifeskim |
pubmed-article:17404368 | lifeskim:mentions | umls-concept:C0085533 | lld:lifeskim |
pubmed-article:17404368 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:17404368 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:17404368 | pubmed:issue | 13 | lld:pubmed |
pubmed-article:17404368 | pubmed:dateCreated | 2007-5-1 | lld:pubmed |
pubmed-article:17404368 | pubmed:abstractText | Southwest Oncology Group (SWOG)/Intergroup study 9623 was undertaken to compare treatment with an anthracycline-based adjuvant chemotherapy regimen followed by high-dose chemotherapy (HDC) with autologous hematopoietic progenitor cell support (AHPCS) with a modern dose-dense dose-escalated (nonstandard) regimen including both an anthracycline and a taxane. | lld:pubmed |
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pubmed-article:17404368 | pubmed:language | eng | lld:pubmed |
pubmed-article:17404368 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17404368 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17404368 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17404368 | pubmed:month | May | lld:pubmed |
pubmed-article:17404368 | pubmed:issn | 1527-7755 | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:GralowJulie... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:LivingstonRob... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:BarlowWilliam... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:BearmanScott... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:IngleJames... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:HudisClifford... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:WolffAntonio... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:ChewHelen KHK | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:MartinoSilvan... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:EliasAnthony... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:LewDanikaD | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:GreenStephani... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:MooreHalle... | lld:pubmed |
pubmed-article:17404368 | pubmed:author | pubmed-author:Southwest... | lld:pubmed |
pubmed-article:17404368 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17404368 | pubmed:day | 1 | lld:pubmed |
pubmed-article:17404368 | pubmed:volume | 25 | lld:pubmed |
pubmed-article:17404368 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17404368 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17404368 | pubmed:pagination | 1677-82 | lld:pubmed |
pubmed-article:17404368 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:meshHeading | pubmed-meshheading:17404368... | lld:pubmed |
pubmed-article:17404368 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17404368 | pubmed:articleTitle | Intensive dose-dense compared with high-dose adjuvant chemotherapy for high-risk operable breast cancer: Southwest Oncology Group/Intergroup study 9623. | lld:pubmed |
pubmed-article:17404368 | pubmed:affiliation | Cleveland Clinic Foundation, Cleveland, OH, USA. | lld:pubmed |
pubmed-article:17404368 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17404368 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:17404368 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:17404368 | pubmed:publicationType | Clinical Trial, Phase III | lld:pubmed |
pubmed-article:17404368 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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