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- Rs7997012 abstract "In genetics, rs7997012 is a gene variation—a single nucleotide polymorphism (SNP)—in intron 2 of the human HTR2A gene that codes for the 5-HT2A receptor.The SNP varies between adenine (A) and guanine (G) DNA bases with the G-allele being most frequent.A research study found it to be related to antidepressant treatment.The research group reported that a polymorphism (rs1954787) on another gene, the GRIK4, has also shown a treatment-response-association in this kind of treatment.In a Japanese study rs7997012 was not associated with neither major depressive disorder nor bipolar disorder.Rs6311, rs6313 and His452Tyr (rs6314) are other SNPs in the HTR2A gene.There are many more, even in intron 2 alone.".
- Rs7997012 wikiPageID "17991482".
- Rs7997012 wikiPageLength "3746".
- Rs7997012 wikiPageOutDegree "17".
- Rs7997012 wikiPageRevisionID "647047609".
- Rs7997012 wikiPageWikiLink 5-HT2A_receptor.
- Rs7997012 wikiPageWikiLink Adenine.
- Rs7997012 wikiPageWikiLink Antidepressant.
- Rs7997012 wikiPageWikiLink Bipolar_disorder.
- Rs7997012 wikiPageWikiLink Category:Single-nucleotide_polymorphisms.
- Rs7997012 wikiPageWikiLink GRIK4.
- Rs7997012 wikiPageWikiLink Gene.
- Rs7997012 wikiPageWikiLink Genetics.
- Rs7997012 wikiPageWikiLink Guanine.
- Rs7997012 wikiPageWikiLink HTR2A.
- Rs7997012 wikiPageWikiLink His452Tyr.
- Rs7997012 wikiPageWikiLink Intron.
- Rs7997012 wikiPageWikiLink Major_depressive_disorder.
- Rs7997012 wikiPageWikiLink Rs1954787.
- Rs7997012 wikiPageWikiLink Rs6311.
- Rs7997012 wikiPageWikiLink Rs6313.
- Rs7997012 wikiPageWikiLink Rs6314.
- Rs7997012 wikiPageWikiLink Single-nucleotide_polymorphism.
- Rs7997012 wikiPageWikiLink Single_nucleotide_polymorphism.
- Rs7997012 wikiPageWikiLinkText "rs7997012".
- Rs7997012 chromosome "13".
- Rs7997012 gene "HTR2A".
- Rs7997012 hasPhotoCollection Rs7997012.
- Rs7997012 region "Intron 2".
- Rs7997012 rsid "7997012".
- Rs7997012 wikiPageUsesTemplate Template:Genetics-stub.
- Rs7997012 wikiPageUsesTemplate Template:Infobox_single_nucleotide_polymorphism.
- Rs7997012 wikiPageUsesTemplate Template:Reflist.
- Rs7997012 subject Category:Single-nucleotide_polymorphisms.
- Rs7997012 hypernym u2014.
- Rs7997012 type Person.
- Rs7997012 comment "In genetics, rs7997012 is a gene variation—a single nucleotide polymorphism (SNP)—in intron 2 of the human HTR2A gene that codes for the 5-HT2A receptor.The SNP varies between adenine (A) and guanine (G) DNA bases with the G-allele being most frequent.A research study found it to be related to antidepressant treatment.The research group reported that a polymorphism (rs1954787) on another gene, the GRIK4, has also shown a treatment-response-association in this kind of treatment.In a Japanese study rs7997012 was not associated with neither major depressive disorder nor bipolar disorder.Rs6311, rs6313 and His452Tyr (rs6314) are other SNPs in the HTR2A gene.There are many more, even in intron 2 alone.".
- Rs7997012 label "Rs7997012".
- Rs7997012 sameAs m.047v32k.
- Rs7997012 sameAs Q7375580.
- Rs7997012 sameAs Q7375580.
- Rs7997012 wasDerivedFrom Rs7997012?oldid=647047609.
- Rs7997012 isPrimaryTopicOf Rs7997012.