| pubmed-article:12671462 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12671462 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:12671462 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:12671462 | lifeskim:mentions | umls-concept:C1417573 | lld:lifeskim |
| pubmed-article:12671462 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:12671462 | lifeskim:mentions | umls-concept:C0181586 | lld:lifeskim |
| pubmed-article:12671462 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:12671462 | pubmed:dateCreated | 2003-4-2 | lld:pubmed |
| pubmed-article:12671462 | pubmed:abstractText | To report a family with a myocilin (MYOC) gene mutation ascertained on the basis of the phenotype of the 71-year-old proband with juvenile-onset primary open-angle glaucoma (JOAG). | lld:pubmed |
| pubmed-article:12671462 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12671462 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12671462 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12671462 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12671462 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12671462 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12671462 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12671462 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12671462 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:12671462 | pubmed:issn | 1057-0829 | lld:pubmed |
| pubmed-article:12671462 | pubmed:author | pubmed-author:RichardsJulia... | lld:pubmed |
| pubmed-article:12671462 | pubmed:author | pubmed-author:LichterPaul... | lld:pubmed |
| pubmed-article:12671462 | pubmed:author | pubmed-author:DownsCatherin... | lld:pubmed |
| pubmed-article:12671462 | pubmed:author | pubmed-author:LimPaulineP | lld:pubmed |
| pubmed-article:12671462 | pubmed:author | pubmed-author:HigashiMisaoM | lld:pubmed |
| pubmed-article:12671462 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12671462 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:12671462 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12671462 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12671462 | pubmed:pagination | 98-103 | lld:pubmed |
| pubmed-article:12671462 | pubmed:dateRevised | 2006-11-3 | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:meshHeading | pubmed-meshheading:12671462... | lld:pubmed |
| pubmed-article:12671462 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:12671462 | pubmed:articleTitle | Septuagenarian's phenotype leads to ascertainment of familial MYOC gene mutation. | lld:pubmed |
| pubmed-article:12671462 | pubmed:affiliation | University of Michigan Medical School, Ann Arbor, Michigan, USA. | lld:pubmed |
| pubmed-article:12671462 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12671462 | pubmed:publicationType | Case Reports | lld:pubmed |
| entrez-gene:4653 | entrezgene:pubmed | pubmed-article:12671462 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:12671462 | lld:entrezgene |
| lhgdn:association:51179 | lhgdn:found_in | pubmed-article:12671462 | lld:lhgdn |
