pubmed-article:14684686 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:14684686 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:14684686 | lifeskim:mentions | umls-concept:C1416525 | lld:lifeskim |
pubmed-article:14684686 | lifeskim:mentions | umls-concept:C0686907 | lld:lifeskim |
pubmed-article:14684686 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:14684686 | pubmed:dateCreated | 2003-12-19 | lld:pubmed |
pubmed-article:14684686 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14684686 | pubmed:abstractText | Alagille syndrome (AGS) is a multi-system, autosomal dominant disorder with highly variable expressivity, caused by mutations within the Jagged1 (JAG1) gene. | lld:pubmed |
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pubmed-article:14684686 | pubmed:language | eng | lld:pubmed |
pubmed-article:14684686 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14684686 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:14684686 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:14684686 | pubmed:month | Dec | lld:pubmed |
pubmed-article:14684686 | pubmed:issn | 1468-6244 | lld:pubmed |
pubmed-article:14684686 | pubmed:author | pubmed-author:SpinnerN BNB | lld:pubmed |
pubmed-article:14684686 | pubmed:author | pubmed-author:BasonLL | lld:pubmed |
pubmed-article:14684686 | pubmed:author | pubmed-author:PiccoliD ADA | lld:pubmed |
pubmed-article:14684686 | pubmed:author | pubmed-author:KrantzI DID | lld:pubmed |
pubmed-article:14684686 | pubmed:author | pubmed-author:KamathB MBM | lld:pubmed |
pubmed-article:14684686 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:14684686 | pubmed:volume | 40 | lld:pubmed |
pubmed-article:14684686 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:14684686 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:14684686 | pubmed:pagination | 891-5 | lld:pubmed |
pubmed-article:14684686 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:14684686 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:14684686 | pubmed:articleTitle | Consequences of JAG1 mutations. | lld:pubmed |
pubmed-article:14684686 | pubmed:affiliation | Division of Gastroenterology, The Children's Hospital of Philadelphia, The University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA. | lld:pubmed |
pubmed-article:14684686 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:14684686 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:14684686 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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