pubmed-article:19956657 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19956657 | lifeskim:mentions | umls-concept:C1412815 | lld:lifeskim |
pubmed-article:19956657 | lifeskim:mentions | umls-concept:C0280100 | lld:lifeskim |
pubmed-article:19956657 | lifeskim:mentions | umls-concept:C0544886 | lld:lifeskim |
pubmed-article:19956657 | lifeskim:mentions | umls-concept:C0038951 | lld:lifeskim |
pubmed-article:19956657 | lifeskim:mentions | umls-concept:C0037791 | lld:lifeskim |
pubmed-article:19956657 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:19956657 | pubmed:dateCreated | 2009-12-3 | lld:pubmed |
pubmed-article:19956657 | pubmed:abstractText | A somatic mutation in the FOXL2 gene is reported to be present in almost all (97%; 86/89) morphologically defined, adult-type, granulosa-cell tumors (A-GCTs). This FOXL2 c.402C>G mutation changes a highly conserved cysteine residue to a tryptophan (p.C134W). It was also found in a minority of other ovarian malignant stromal tumors, but not in benign ovarian stromal tumors or unrelated ovarian tumors or breast cancers. | lld:pubmed |
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pubmed-article:19956657 | pubmed:language | eng | lld:pubmed |
pubmed-article:19956657 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19956657 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:19956657 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19956657 | pubmed:issn | 1932-6203 | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:MonahanJohnJ | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:BrentonJames... | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:GilksC... | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:HuntsmanDavid... | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:LeungPeterP | lld:pubmed |
pubmed-article:19956657 | pubmed:author | pubmed-author:SenzJanineJ | lld:pubmed |
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pubmed-article:19956657 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19956657 | pubmed:volume | 4 | lld:pubmed |
pubmed-article:19956657 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19956657 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19956657 | pubmed:pagination | e7988 | lld:pubmed |
pubmed-article:19956657 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
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pubmed-article:19956657 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19956657 | pubmed:articleTitle | The specificity of the FOXL2 c.402C>G somatic mutation: a survey of solid tumors. | lld:pubmed |
pubmed-article:19956657 | pubmed:affiliation | Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada. | lld:pubmed |
pubmed-article:19956657 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19956657 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:668 | entrezgene:pubmed | pubmed-article:19956657 | lld:entrezgene |
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