| pubmed-article:15146436 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C1368019 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C2745955 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C1420393 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:15146436 | lifeskim:mentions | umls-concept:C0027778 | lld:lifeskim |
| pubmed-article:15146436 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:15146436 | pubmed:dateCreated | 2004-5-17 | lld:pubmed |
| pubmed-article:15146436 | pubmed:abstractText | To estimate the occurrence of familial Paget's disease of bone in The Netherlands, to examine the prevalence of mutations of the sequestosome 1 gene (SQSTM1) in identified families, and to assess potential genotype-phenotype associations. | lld:pubmed |
| pubmed-article:15146436 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15146436 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:15146436 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15146436 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15146436 | pubmed:month | May | lld:pubmed |
| pubmed-article:15146436 | pubmed:issn | 0004-3591 | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:PapapoulosS... | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:ZwindermanA... | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:KarperienMM | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:DragoiescuCC | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:KneppersA L... | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:EekhoffE W... | lld:pubmed |
| pubmed-article:15146436 | pubmed:author | pubmed-author:HoutsmaDD | lld:pubmed |
| pubmed-article:15146436 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15146436 | pubmed:volume | 50 | lld:pubmed |
| pubmed-article:15146436 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15146436 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15146436 | pubmed:pagination | 1650-4 | lld:pubmed |
| pubmed-article:15146436 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:meshHeading | pubmed-meshheading:15146436... | lld:pubmed |
| pubmed-article:15146436 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15146436 | pubmed:articleTitle | Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations. | lld:pubmed |
| pubmed-article:15146436 | pubmed:affiliation | Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands. | lld:pubmed |
| pubmed-article:15146436 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15146436 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:8878 | entrezgene:pubmed | pubmed-article:15146436 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:15146436 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15146436 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15146436 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15146436 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15146436 | lld:pubmed |
