pubmed-article:12821254 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C1710961 | lld:lifeskim |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C0152171 | lld:lifeskim |
pubmed-article:12821254 | lifeskim:mentions | umls-concept:C0019409 | lld:lifeskim |
pubmed-article:12821254 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:12821254 | pubmed:dateCreated | 2003-6-24 | lld:pubmed |
pubmed-article:12821254 | pubmed:abstractText | The aim of our study was to identify genetic causes of primary pulmonary hypertension (PPH), to estimate the proportion of families with mutations in the BMPR2 (bone morphogenetic protein receptor type 2) gene, and to examine whether genetic heterogeneity might play a role. | lld:pubmed |
pubmed-article:12821254 | pubmed:language | eng | lld:pubmed |
pubmed-article:12821254 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12821254 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:12821254 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12821254 | pubmed:month | Jun | lld:pubmed |
pubmed-article:12821254 | pubmed:issn | 0735-1097 | lld:pubmed |
pubmed-article:12821254 | pubmed:author | pubmed-author:HoeperMarius... | lld:pubmed |
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pubmed-article:12821254 | pubmed:author | pubmed-author:WinklerJörgJ | lld:pubmed |
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pubmed-article:12821254 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12821254 | pubmed:day | 18 | lld:pubmed |
pubmed-article:12821254 | pubmed:volume | 41 | lld:pubmed |
pubmed-article:12821254 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12821254 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12821254 | pubmed:pagination | 2237-44 | lld:pubmed |
pubmed-article:12821254 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:12821254 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12821254 | pubmed:articleTitle | Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31. | lld:pubmed |
pubmed-article:12821254 | pubmed:affiliation | Institute of Human Genetics, University of Heidelberg, Germany. | lld:pubmed |
pubmed-article:12821254 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12821254 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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