Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Rs1800532> ?p ?o }
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- Rs1800532 abstract "In genetics, rs1800532 (A218C) is a genetic variant.It is a single nucleotide polymorphism in the TPH1 gene and located in intron 7.It has been examined in relation to personality traits.A779C is another SNP in same intron.".
- Rs1800532 wikiPageID "19438297".
- Rs1800532 wikiPageLength "1908".
- Rs1800532 wikiPageOutDegree "8".
- Rs1800532 wikiPageRevisionID "594977835".
- Rs1800532 wikiPageWikiLink Category:Single-nucleotide_polymorphisms.
- Rs1800532 wikiPageWikiLink Gene.
- Rs1800532 wikiPageWikiLink Genetics.
- Rs1800532 wikiPageWikiLink Intron.
- Rs1800532 wikiPageWikiLink Personality_trait.
- Rs1800532 wikiPageWikiLink Rs1799913.
- Rs1800532 wikiPageWikiLink Single-nucleotide_polymorphism.
- Rs1800532 wikiPageWikiLink Single_nucleotide_polymorphism.
- Rs1800532 wikiPageWikiLink TPH1.
- Rs1800532 wikiPageWikiLink Trait_theory.
- Rs1800532 wikiPageWikiLinkText "Rs1800532".
- Rs1800532 wikiPageWikiLinkText "rs1800532".
- Rs1800532 chromosome "11".
- Rs1800532 gene "TPH1".
- Rs1800532 hasPhotoCollection Rs1800532.
- Rs1800532 name "A218C".
- Rs1800532 region "Intron 7".
- Rs1800532 rsid "1800532".
- Rs1800532 wikiPageUsesTemplate Template:Infobox_single_nucleotide_polymorphism.
- Rs1800532 wikiPageUsesTemplate Template:Reflist.
- Rs1800532 subject Category:Single-nucleotide_polymorphisms.
- Rs1800532 hypernym Variant.
- Rs1800532 comment "In genetics, rs1800532 (A218C) is a genetic variant.It is a single nucleotide polymorphism in the TPH1 gene and located in intron 7.It has been examined in relation to personality traits.A779C is another SNP in same intron.".
- Rs1800532 label "Rs1800532".
- Rs1800532 sameAs m.04n2njt.
- Rs1800532 sameAs Rs1800532.
- Rs1800532 sameAs Q4048577.
- Rs1800532 sameAs Q4048577.
- Rs1800532 wasDerivedFrom Rs1800532?oldid=594977835.
- Rs1800532 isPrimaryTopicOf Rs1800532.