Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Rs1801133> ?p ?o }
Showing triples 1 to 43 of
43
with 100 triples per page.
- Rs1801133 abstract "C677T or Rs1801133 is a genetic variation—a single nucleotide polymorphism (SNP)—in the MTHFR gene.Among Americans the frequency of T-homozygosity ranges from 1% or less among Blacks to 20% or more among Italians and Hispanics.It has been related to schizophrenia Alzheimer's disease depression autism spina bifida.In 2000 association studies on oral clefts, Down syndrome, and fetal anticonvulsant syndrome were either unreplicated or had yielded conflicting results.".
- Rs1801133 wikiPageID "18688564".
- Rs1801133 wikiPageLength "3498".
- Rs1801133 wikiPageOutDegree "12".
- Rs1801133 wikiPageRevisionID "703112668".
- Rs1801133 wikiPageWikiLink A1298C.
- Rs1801133 wikiPageWikiLink Alzheimers_disease.
- Rs1801133 wikiPageWikiLink Autism.
- Rs1801133 wikiPageWikiLink Category:Single-nucleotide_polymorphisms.
- Rs1801133 wikiPageWikiLink Down_syndrome.
- Rs1801133 wikiPageWikiLink Fetal_anticonvulsant_syndrome.
- Rs1801133 wikiPageWikiLink Gene.
- Rs1801133 wikiPageWikiLink Methylenetetrahydrofolate_reductase.
- Rs1801133 wikiPageWikiLink Oral_cleft.
- Rs1801133 wikiPageWikiLink Schizophrenia.
- Rs1801133 wikiPageWikiLink Single-nucleotide_polymorphism.
- Rs1801133 wikiPageWikiLink Spina_bifida.
- Rs1801133 wikiPageWikiLinkText "MTHFR 677T".
- Rs1801133 wikiPageWikiLinkText "Rs1801133".
- Rs1801133 wikiPageWikiLinkText "rs1801133".
- Rs1801133 alzgeneGeneid "70".
- Rs1801133 alzgenePolyid "155".
- Rs1801133 chromosome "1".
- Rs1801133 gene "MTHFR".
- Rs1801133 name "A222V".
- Rs1801133 name "Ala222Val".
- Rs1801133 name "C677T".
- Rs1801133 rsid "1801133".
- Rs1801133 szgeneGeneid "4".
- Rs1801133 szgenePolyid "31".
- Rs1801133 wikiPageUsesTemplate Template:Infobox_single_nucleotide_polymorphism.
- Rs1801133 wikiPageUsesTemplate Template:Reflist.
- Rs1801133 subject Category:Single-nucleotide_polymorphisms.
- Rs1801133 hypernym —.
- Rs1801133 type Work.
- Rs1801133 comment "C677T or Rs1801133 is a genetic variation—a single nucleotide polymorphism (SNP)—in the MTHFR gene.Among Americans the frequency of T-homozygosity ranges from 1% or less among Blacks to 20% or more among Italians and Hispanics.It has been related to schizophrenia Alzheimer's disease depression autism spina bifida.In 2000 association studies on oral clefts, Down syndrome, and fetal anticonvulsant syndrome were either unreplicated or had yielded conflicting results.".
- Rs1801133 label "Rs1801133".
- Rs1801133 sameAs Q4048578.
- Rs1801133 sameAs m.04gljmg.
- Rs1801133 sameAs Rs1801133.
- Rs1801133 sameAs Q4048578.
- Rs1801133 wasDerivedFrom Rs1801133?oldid=703112668.
- Rs1801133 isPrimaryTopicOf Rs1801133.