pubmed-article:18833581 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C0042610 | lld:lifeskim |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C0043027 | lld:lifeskim |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C0038436 | lld:lifeskim |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C1333253 | lld:lifeskim |
pubmed-article:18833581 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
pubmed-article:18833581 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:18833581 | pubmed:dateCreated | 2009-1-22 | lld:pubmed |
pubmed-article:18833581 | pubmed:abstractText | Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic Stress Disorder (PTSD). A single nucleotide polymorphism (SNP) (957C>T) and a deletion polymorphism (-141delC) in the DRD2 gene and a SNP (Taq1A) in a gene directly downstream of DRD2 have all been implicated in dopamine functioning in the brain. | lld:pubmed |
pubmed-article:18833581 | pubmed:language | eng | lld:pubmed |
pubmed-article:18833581 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18833581 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18833581 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18833581 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18833581 | pubmed:issn | 1520-6394 | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:VoiseyJoanneJ | lld:pubmed |
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pubmed-article:18833581 | pubmed:author | pubmed-author:KannBurnettB | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:HughesIan PIP | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:SwagellChrist... | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:MorrisC... | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:NobleEarnest... | lld:pubmed |
pubmed-article:18833581 | pubmed:author | pubmed-author:HeslopKaren... | lld:pubmed |
pubmed-article:18833581 | pubmed:copyrightInfo | (c) 2008 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:18833581 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18833581 | pubmed:volume | 26 | lld:pubmed |
pubmed-article:18833581 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18833581 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18833581 | pubmed:pagination | 28-33 | lld:pubmed |
pubmed-article:18833581 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:18833581 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:18833581 | pubmed:articleTitle | The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans. | lld:pubmed |
pubmed-article:18833581 | pubmed:affiliation | Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, Australia. j.voisey@qut.edu.au | lld:pubmed |
pubmed-article:18833581 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18833581 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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