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- Rs6295 abstract "rs6295, also called C(-1019)G, is a gene variation—a single nucleotide polymorphism (SNP)—in the HTR1A gene. It is one of the most investigated SNPs of its gene. The C-allele is the most prevalent with 0.675 against the G-allele with 0.325 among Caucasian.The effect of the SNP on the binding potential of the human 5-HT1A neuroreceptor has been assessed with positron emission tomography and the WAY-100635 radioligand, with a study reporting no apparent influence from the SNP.".
- Rs6295 wikiPageID "17870559".
- Rs6295 wikiPageLength "7340".
- Rs6295 wikiPageOutDegree "31".
- Rs6295 wikiPageRevisionID "672943860".
- Rs6295 wikiPageWikiLink 5-HT1A_receptor.
- Rs6295 wikiPageWikiLink 5-HT2A_receptor.
- Rs6295 wikiPageWikiLink Allele.
- Rs6295 wikiPageWikiLink Antidepressant.
- Rs6295 wikiPageWikiLink Binding_potential.
- Rs6295 wikiPageWikiLink C549T.
- Rs6295 wikiPageWikiLink Category:Single-nucleotide_polymorphisms.
- Rs6295 wikiPageWikiLink Caucasian_race.
- Rs6295 wikiPageWikiLink G294A.
- Rs6295 wikiPageWikiLink Gene.
- Rs6295 wikiPageWikiLink Gly272Asp.
- Rs6295 wikiPageWikiLink HTR1A.
- Rs6295 wikiPageWikiLink Harm_Avoidance.
- Rs6295 wikiPageWikiLink Harm_avoidance.
- Rs6295 wikiPageWikiLink Ile28Val.
- Rs6295 wikiPageWikiLink Major_depression.
- Rs6295 wikiPageWikiLink Major_depressive_disorder.
- Rs6295 wikiPageWikiLink Mental_disorder.
- Rs6295 wikiPageWikiLink Mood_disorder.
- Rs6295 wikiPageWikiLink NEO_PI-R.
- Rs6295 wikiPageWikiLink Neuroticism.
- Rs6295 wikiPageWikiLink Personality_trait.
- Rs6295 wikiPageWikiLink Positron_emission_tomography.
- Rs6295 wikiPageWikiLink Premenstrual_dysphoric_disorder.
- Rs6295 wikiPageWikiLink Pro16Leu.
- Rs6295 wikiPageWikiLink Psychiatric_disorder.
- Rs6295 wikiPageWikiLink Radioligand.
- Rs6295 wikiPageWikiLink Revised_NEO_Personality_Inventory.
- Rs6295 wikiPageWikiLink Rs6294.
- Rs6295 wikiPageWikiLink Schizophrenia.
- Rs6295 wikiPageWikiLink Self-transcendence.
- Rs6295 wikiPageWikiLink Single-nucleotide_polymorphism.
- Rs6295 wikiPageWikiLink Single_nucleotide_polymorphism.
- Rs6295 wikiPageWikiLink Suicide.
- Rs6295 wikiPageWikiLink Temperament_and_Character_Inventory.
- Rs6295 wikiPageWikiLink Trait_theory.
- Rs6295 wikiPageWikiLink Tridimensional_Personality_Questionnaire.
- Rs6295 wikiPageWikiLink WAY-100,635.
- Rs6295 wikiPageWikiLink WAY-100635.
- Rs6295 wikiPageWikiLinkText "Rs6295".
- Rs6295 wikiPageWikiLinkText "rs6295".
- Rs6295 chromosome "5".
- Rs6295 gene "HTR1A".
- Rs6295 hasPhotoCollection Rs6295.
- Rs6295 name "C-1019G".
- Rs6295 name "CG".
- Rs6295 personalitystudyGenotype "G".
- Rs6295 personalitystudyInventory "NEO PI-R".
- Rs6295 personalitystudyInventory "TPQ".
- Rs6295 personalitystudyPmid "14666415".
- Rs6295 personalitystudyTrait "Harm Avoidance".
- Rs6295 personalitystudyTrait "Neuroticism".
- Rs6295 region "Promoter".
- Rs6295 rsid "6295".
- Rs6295 wikiPageUsesTemplate Template:Infobox_single_nucleotide_polymorphism.
- Rs6295 wikiPageUsesTemplate Template:Reflist.
- Rs6295 wikiPageUsesTemplate Template:Use_dmy_dates.
- Rs6295 subject Category:Single-nucleotide_polymorphisms.
- Rs6295 hypernym u2014.
- Rs6295 type Person.
- Rs6295 comment "rs6295, also called C(-1019)G, is a gene variation—a single nucleotide polymorphism (SNP)—in the HTR1A gene. It is one of the most investigated SNPs of its gene. The C-allele is the most prevalent with 0.675 against the G-allele with 0.325 among Caucasian.The effect of the SNP on the binding potential of the human 5-HT1A neuroreceptor has been assessed with positron emission tomography and the WAY-100635 radioligand, with a study reporting no apparent influence from the SNP.".
- Rs6295 label "Rs6295".
- Rs6295 sameAs m.047fytm.
- Rs6295 sameAs Q7375575.
- Rs6295 sameAs Q7375575.
- Rs6295 wasDerivedFrom Rs6295?oldid=672943860.
- Rs6295 isPrimaryTopicOf Rs6295.