| pubmed-article:18827002 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18827002 | lifeskim:mentions | umls-concept:C0014130 | lld:lifeskim |
| pubmed-article:18827002 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:18827002 | lifeskim:mentions | umls-concept:C2735448 | lld:lifeskim |
| pubmed-article:18827002 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:18827002 | pubmed:dateCreated | 2008-12-5 | lld:pubmed |
| pubmed-article:18827002 | pubmed:abstractText | Familial clustering of a disease is an indicator of a possible heritable cause. In the era of genome scans, the consideration of data on heritability should be important in the assessment of the likely success of the scans. | lld:pubmed |
| pubmed-article:18827002 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18827002 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18827002 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:18827002 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18827002 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:18827002 | pubmed:issn | 0021-972X | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:HemminkiKariK | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:LiXinjunX | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:SundquistJanJ | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:ShuXiaochenX | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:SundquistKris... | lld:pubmed |
| pubmed-article:18827002 | pubmed:author | pubmed-author:JiJianguangJ | lld:pubmed |
| pubmed-article:18827002 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18827002 | pubmed:volume | 93 | lld:pubmed |
| pubmed-article:18827002 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18827002 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18827002 | pubmed:pagination | 4755-8 | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
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| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:meshHeading | pubmed-meshheading:18827002... | lld:pubmed |
| pubmed-article:18827002 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18827002 | pubmed:articleTitle | Familial risks for hospitalization with endocrine diseases. | lld:pubmed |
| pubmed-article:18827002 | pubmed:affiliation | Division of Molecular Genetic Epidemiology, German Cancer Research Center, Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany. k.hemminki@dkfz.de | lld:pubmed |
| pubmed-article:18827002 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18827002 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
