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| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0376358 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0029246 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0035168 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0016384 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0032952 | lld:lifeskim |
| pubmed-article:11134196 | lifeskim:mentions | umls-concept:C0282461 | lld:lifeskim |
| pubmed-article:11134196 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:11134196 | pubmed:dateCreated | 2001-1-26 | lld:pubmed |
| pubmed-article:11134196 | pubmed:abstractText | Time to progression (TTP), overall survival, and quality of life (QL) were compared in patients with hormone-resistant prostate cancer (HRPC) treated with prednisone (5 mg orally, four times a day) or flutamide (250 mg orally, three times a day). | lld:pubmed |
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| pubmed-article:11134196 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11134196 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11134196 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:11134196 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11134196 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:11134196 | pubmed:issn | 0732-183X | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:FossåS DSD | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:HallR RRR | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:SleeP HPH | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:HorenblasSS | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:AaronsonNN | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:BrausiMM | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:CollettiPP | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:HetheringtonJ... | lld:pubmed |
| pubmed-article:11134196 | pubmed:author | pubmed-author:de Prijck L | lld:pubmed |
| pubmed-article:11134196 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11134196 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:11134196 | pubmed:volume | 19 | lld:pubmed |
| pubmed-article:11134196 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11134196 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11134196 | pubmed:pagination | 62-71 | lld:pubmed |
| pubmed-article:11134196 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:11134196 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11134196 | pubmed:articleTitle | Flutamide versus prednisone in patients with prostate cancer symptomatically progressing after androgen-ablative therapy: a phase III study of the European organization for research and treatment of cancer genitourinary group. | lld:pubmed |
| pubmed-article:11134196 | pubmed:affiliation | Department of Medical Oncology and Radiotherapy, Norwegian Radium Hospital, Oslo, Norway. s.d.fossa@klinmed.uio.no | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Multicenter Study | lld:pubmed |
| pubmed-article:11134196 | pubmed:publicationType | Clinical Trial, Phase III | lld:pubmed |
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