| pubmed-article:16129848 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C1513906 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C0684224 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C0027708 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C1327810 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C1520690 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C0524869 | lld:lifeskim |
| pubmed-article:16129848 | lifeskim:mentions | umls-concept:C1514474 | lld:lifeskim |
| pubmed-article:16129848 | pubmed:issue | 29 | lld:pubmed |
| pubmed-article:16129848 | pubmed:dateCreated | 2005-10-7 | lld:pubmed |
| pubmed-article:16129848 | pubmed:abstractText | To determine if tumor-specific loss of heterozygosity (LOH) for chromosomes 1p or 16q is associated with a poorer prognosis for children with favorable-histology (FH) Wilms tumor entered on the fifth National Wilms Tumor Study (NWTS-5). | lld:pubmed |
| pubmed-article:16129848 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16129848 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16129848 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16129848 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16129848 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16129848 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:16129848 | pubmed:issn | 0732-183X | lld:pubmed |
| pubmed-article:16129848 | pubmed:author | pubmed-author:GrundyPaul... | lld:pubmed |
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| pubmed-article:16129848 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16129848 | pubmed:day | 10 | lld:pubmed |
| pubmed-article:16129848 | pubmed:volume | 23 | lld:pubmed |
| pubmed-article:16129848 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16129848 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16129848 | pubmed:pagination | 7312-21 | lld:pubmed |
| pubmed-article:16129848 | pubmed:dateRevised | 2009-11-3 | lld:pubmed |
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| pubmed-article:16129848 | pubmed:meshHeading | pubmed-meshheading:16129848... | lld:pubmed |
| pubmed-article:16129848 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16129848 | pubmed:articleTitle | Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group. | lld:pubmed |
| pubmed-article:16129848 | pubmed:affiliation | Department of Pediatrics, Roswell Park Cancer Institute, Taipei. pgrundy@cha.ab.ca | lld:pubmed |
| pubmed-article:16129848 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16129848 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| pubmed-article:16129848 | pubmed:publicationType | Multicenter Study | lld:pubmed |
| pubmed-article:16129848 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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