| pubmed-article:21204696 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C0034818 | lld:lifeskim |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C1334140 | lld:lifeskim |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C0123658 | lld:lifeskim |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C1954276 | lld:lifeskim |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:21204696 | lifeskim:mentions | umls-concept:C0031928 | lld:lifeskim |
| pubmed-article:21204696 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:21204696 | pubmed:dateCreated | 2011-2-28 | lld:pubmed |
| pubmed-article:21204696 | pubmed:abstractText | In recent years, numerous studies have focused their attention on genes that are part of the insulin/insulin-like growth factor 1 signaling pathway, such as the insulin receptor (INSR) and the insulin receptor substrate 1 (IRS1) genes. | lld:pubmed |
| pubmed-article:21204696 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21204696 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21204696 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21204696 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21204696 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21204696 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21204696 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:21204696 | pubmed:issn | 1945-0257 | lld:pubmed |
| pubmed-article:21204696 | pubmed:author | pubmed-author:ReljicAnteA | lld:pubmed |
| pubmed-article:21204696 | pubmed:author | pubmed-author:SimundicAna-M... | lld:pubmed |
| pubmed-article:21204696 | pubmed:author | pubmed-author:NikolacNoraN | lld:pubmed |
| pubmed-article:21204696 | pubmed:author | pubmed-author:SaracevicAndr... | lld:pubmed |
| pubmed-article:21204696 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21204696 | pubmed:volume | 15 | lld:pubmed |
| pubmed-article:21204696 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21204696 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21204696 | pubmed:pagination | 127-31 | lld:pubmed |
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| pubmed-article:21204696 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21204696 | pubmed:articleTitle | Insulin receptor H1085H C>T and insulin receptor substrate 1 G972R polymorphisms and prostate cancer risk: a pilot study. | lld:pubmed |
| pubmed-article:21204696 | pubmed:affiliation | University Department of Chemistry, Sestre Milosrdnice University Hospital, Zagreb, Croatia. andrea.saracevic@gmail.com | lld:pubmed |
| pubmed-article:21204696 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21204696 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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