| pubmed-article:18424907 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C0007407 | lld:lifeskim |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C0036341 | lld:lifeskim |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C0686347 | lld:lifeskim |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:18424907 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:18424907 | pubmed:issue | 1-2 | lld:pubmed |
| pubmed-article:18424907 | pubmed:dateCreated | 2008-6-19 | lld:pubmed |
| pubmed-article:18424907 | pubmed:abstractText | This study investigated whether the catechol-O-methyltransferase (COMT) gene V158M single-nucleotide polymorphism (SNP) influences susceptibility to tardive dyskinesia (TD). | lld:pubmed |
| pubmed-article:18424907 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18424907 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18424907 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18424907 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18424907 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18424907 | pubmed:issn | 1423-0224 | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:KimYong-KuYK | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:LeeMin-SooMS | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:ParkYoung-Min... | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:OURY | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:KimSeung-Hyun... | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:LeeHeon-Jeong... | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:JoeSook-Haeng... | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:JungIn-KwaIK | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:HanChangsuC | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:KangSeung-Gul... | lld:pubmed |
| pubmed-article:18424907 | pubmed:author | pubmed-author:ChoiJung-EunJ... | lld:pubmed |
| pubmed-article:18424907 | pubmed:copyrightInfo | 2008 S. Karger AG, Basel. | lld:pubmed |
| pubmed-article:18424907 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18424907 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:18424907 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18424907 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18424907 | pubmed:pagination | 22-5 | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:meshHeading | pubmed-meshheading:18424907... | lld:pubmed |
| pubmed-article:18424907 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18424907 | pubmed:articleTitle | Val158Met polymorphism in the catechol-O-methyltransferase (COMT) gene is not associated with tardive dyskinesia in schizophrenia. | lld:pubmed |
| pubmed-article:18424907 | pubmed:affiliation | Department of Psychiatry, Korea University College of Medicine, Seoul, South Korea. | lld:pubmed |
| pubmed-article:18424907 | pubmed:publicationType | Journal Article | lld:pubmed |
| entrez-gene:1312 | entrezgene:pubmed | pubmed-article:18424907 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18424907 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18424907 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18424907 | lld:pubmed |
