21192222

Source:http://linkedlifedata.com/resource/pubmed/id/21192222

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0086982, umls-concept:C0205419, umls-concept:C0314603, umls-concept:C0332281, umls-concept:C0410702, umls-concept:C1156659
pubmed:issue	1
pubmed:dateCreated	2010-12-30
pubmed:abstractText	Genetic association study investigating the association of genetic markers of melatonin signaling and biosynthesis with adolescent idiopathic scoliosis (AIS).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7610646
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Acetylserotonin O-Methyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Arylalkylamine N-Acetyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Melatonin, http://linkedlifedata.com/resource/pubmed/chemical/PRKCD protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C-delta, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Melatonin, MT1, http://linkedlifedata.com/resource/pubmed/chemical/TPH1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Tryptophan Hydroxylase
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1528-1159
pubmed:author	pubmed-author:NelsonLesa MLM, pubmed-author:OgilvieJames WJW, pubmed-author:WardKennethK
pubmed:issnType	Electronic
pubmed:day	1
pubmed:volume	36
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	37-40
pubmed:meshHeading	pubmed-meshheading:21192222-Acetylserotonin O-Methyltransferase, pubmed-meshheading:21192222-Adolescent, pubmed-meshheading:21192222-Arylalkylamine N-Acetyltransferase, pubmed-meshheading:21192222-Case-Control Studies, pubmed-meshheading:21192222-Chi-Square Distribution, pubmed-meshheading:21192222-Gene Frequency, pubmed-meshheading:21192222-Genetic Association Studies, pubmed-meshheading:21192222-Genetic Predisposition to Disease, pubmed-meshheading:21192222-High-Throughput Nucleotide Sequencing, pubmed-meshheading:21192222-Humans, pubmed-meshheading:21192222-Melatonin, pubmed-meshheading:21192222-Odds Ratio, pubmed-meshheading:21192222-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:21192222-Phenotype, pubmed-meshheading:21192222-Polymorphism, Single Nucleotide, pubmed-meshheading:21192222-Protein Kinase C-delta, pubmed-meshheading:21192222-Receptor, Melatonin, MT1, pubmed-meshheading:21192222-Risk Assessment, pubmed-meshheading:21192222-Risk Factors, pubmed-meshheading:21192222-Scoliosis, pubmed-meshheading:21192222-Signal Transduction, pubmed-meshheading:21192222-Tryptophan Hydroxylase, pubmed-meshheading:21192222-United States
pubmed:year	2011
pubmed:articleTitle	Genetic variants in melatonin synthesis and signaling pathway are not associated with adolescent idiopathic scoliosis.
pubmed:affiliation	Axial Biotech, Inc, Salt Lake City, Utah, USA. lnelson@axialbiotech.com
pubmed:publicationType	Journal Article