21342622

Source:http://linkedlifedata.com/resource/pubmed/id/21342622

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008059, umls-concept:C1135159, umls-concept:C1263846, umls-concept:C1882417
pubmed:issue	2
pubmed:dateCreated	2011-2-23
pubmed:abstractText	To study the relationship between rs6267 polymorphism of catechol-O-methyltransferase (COMT) gene and attention deficit hyperactivity disorder (ADHD).
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100909956
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Catechol O-Methyltransferase
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1008-8830
pubmed:author	pubmed-author:ChenLei-YinLY, pubmed-author:LuoXue-RongXR, pubmed-author:SzuS SSS, pubmed-author:ZhangYue-BingYB, pubmed-author:ZhongYanY, pubmed-author:ZhuFengF
pubmed:issnType	Print
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	127-30
pubmed:meshHeading	pubmed-meshheading:21342622-Adolescent, pubmed-meshheading:21342622-Attention Deficit Disorder with Hyperactivity, pubmed-meshheading:21342622-Catechol O-Methyltransferase, pubmed-meshheading:21342622-Child, pubmed-meshheading:21342622-Female, pubmed-meshheading:21342622-Gene Frequency, pubmed-meshheading:21342622-Genetic Predisposition to Disease, pubmed-meshheading:21342622-Genotype, pubmed-meshheading:21342622-Humans, pubmed-meshheading:21342622-Male, pubmed-meshheading:21342622-Polymorphism, Genetic
pubmed:year	2011
pubmed:articleTitle	[Catechol-O-methyltransferase gene rs6267 polymorphism in children with attention deficit hyperactivity disorder].
pubmed:affiliation	Mental Health Institute, Second Xiangya Hospital, Central South University, Changsha 410011, China.
pubmed:publicationType	Journal Article, English Abstract, Research Support, Non-U.S. Gov't