| pubmed-article:21255467 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C1335929 | lld:lifeskim |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C0292369 | lld:lifeskim |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C0812273 | lld:lifeskim |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C0205422 | lld:lifeskim |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C0206530 | lld:lifeskim |
| pubmed-article:21255467 | lifeskim:mentions | umls-concept:C1880177 | lld:lifeskim |
| pubmed-article:21255467 | pubmed:dateCreated | 2011-2-14 | lld:pubmed |
| pubmed-article:21255467 | pubmed:abstractText | Schwannomatosis is a disease characterized by multiple non-vestibular schwannomas. Although biallelic NF2 mutations are found in schwannomas, no germ line event is detected in schwannomatosis patients. In contrast, germline mutations of the SMARCB1 (INI1) tumor suppressor gene were described in familial and sporadic schwannomatosis patients. | lld:pubmed |
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| pubmed-article:21255467 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21255467 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21255467 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21255467 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:21255467 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21255467 | pubmed:issn | 1471-2377 | lld:pubmed |
| pubmed-article:21255467 | pubmed:author | pubmed-author:SobolHagayH | lld:pubmed |
| pubmed-article:21255467 | pubmed:author | pubmed-author:NoguchiTetsur... | lld:pubmed |
| pubmed-article:21255467 | pubmed:author | pubmed-author:OlschwangSylv... | lld:pubmed |
| pubmed-article:21255467 | pubmed:author | pubmed-author:BourdonViolai... | lld:pubmed |
| pubmed-article:21255467 | pubmed:author | pubmed-author:RousseauGuill... | lld:pubmed |
| pubmed-article:21255467 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21255467 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:21255467 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21255467 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21255467 | pubmed:pagination | 9 | lld:pubmed |
| pubmed-article:21255467 | pubmed:dateRevised | 2011-7-25 | lld:pubmed |
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| pubmed-article:21255467 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21255467 | pubmed:articleTitle | SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis. | lld:pubmed |
| pubmed-article:21255467 | pubmed:affiliation | Laboratory of Molecular Oncogenetics, Institut Paoli-Calmettes, Marseille, France. | lld:pubmed |
| pubmed-article:21255467 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21255467 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:6598 | entrezgene:pubmed | pubmed-article:21255467 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21255467 | lld:entrezgene |
