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- Rs1799913 abstract "In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene.It is located in intron 7.The SNP association with schizophrenia has been examined in several studies, though as of 2007 with no definitive conclusion.One study has found that the SNP may be associated with heroin addiction.A218C (rs1800532) is another SNP in the same intron in the same gene.".
- Rs1799913 wikiPageID "18158692".
- Rs1799913 wikiPageRevisionID "594977830".
- Rs1799913 chromosome "11".
- Rs1799913 gene "TPH1".
- Rs1799913 hasPhotoCollection Rs1799913.
- Rs1799913 name "A779C".
- Rs1799913 region "Intron 7".
- Rs1799913 rsid "1799913".
- Rs1799913 szgeneGeneid "111".
- Rs1799913 szgenePolyid "586".
- Rs1799913 subject Category:Single-nucleotide_polymorphisms.
- Rs1799913 comment "In genetics, rs1799913, also called A779C, is a gene variation—a single nucleotide polymorphism (SNP)— in the TPH1 gene.It is located in intron 7.The SNP association with schizophrenia has been examined in several studies, though as of 2007 with no definitive conclusion.One study has found that the SNP may be associated with heroin addiction.A218C (rs1800532) is another SNP in the same intron in the same gene.".
- Rs1799913 label "Rs1799913".
- Rs1799913 label "Rs1799913".
- Rs1799913 sameAs m.04cxw0j.
- Rs1799913 sameAs Q4048575.
- Rs1799913 sameAs Q4048575.
- Rs1799913 wasDerivedFrom Rs1799913?oldid=594977830.
- Rs1799913 isPrimaryTopicOf Rs1799913.