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- Q4048578 subject Q7478152.
- Q4048578 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.".
- Q4048578 wikiPageWikiLink Q11081.
- Q4048578 wikiPageWikiLink Q14864922.
- Q4048578 wikiPageWikiLink Q38404.
- Q4048578 wikiPageWikiLink Q41112.
- Q4048578 wikiPageWikiLink Q47715.
- Q4048578 wikiPageWikiLink Q501128.
- Q4048578 wikiPageWikiLink Q7187.
- Q4048578 wikiPageWikiLink Q7478152.
- Q4048578 wikiPageWikiLink Q844717.
- Q4048578 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.".
- Q4048578 label "Rs1801133".