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- NCIT_C49357 IAO_0000115 "Human EPHX1 wild-type allele is located in the vicinity of 1q42.1 and is approximately 35 kb in length. This allele, which encodes epoxide hydrolase 1 protein, is involved in the metabolism of both arene and aliphatic epoxides. Certain allelic variants of the EPHX1 gene confer susceptibility to lymphoproliferative disorders. Specific inherited defects in this gene also cause familial hypercholanemia. An EPHX1 low-activity genotype is associated with decreased risk of lung cancer." @default.
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- NCIT_C49357 NCIT_P100 "132810" @default.
- NCIT_C49357 NCIT_P102 "NM_000120" @default.
- NCIT_C49357 NCIT_P106 "Gene or Genome" @default.
- NCIT_C49357 NCIT_P108 "EPHX1 wt Allele" @default.
- NCIT_C49357 NCIT_P207 "C1705462" @default.
- NCIT_C49357 NCIT_P211 "epoxide hydrolase activity" @default.
- NCIT_C49357 NCIT_P321 "2052" @default.
- NCIT_C49357 NCIT_P366 "EPHX1_wt_Allele" @default.
- NCIT_C49357 NCIT_P96 "Microsomal Epoxide Hydrolase" @default.
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- NCIT_C49357 normalizedInformationContent "100" @default.
- NCIT_C49357 referenceCount "1" @default.
- NCIT_C49357 hasExactSynonym "EPHX" @default.
- NCIT_C49357 hasExactSynonym "EPHX1 wt Allele" @default.
- NCIT_C49357 hasExactSynonym "EPOX" @default.
- NCIT_C49357 hasExactSynonym "Epoxide Hydrolase 1, Microsomal (Xenobiotic) wt Allele" @default.
- NCIT_C49357 hasExactSynonym "MEH" @default.
- NCIT_C49357 type Class @default.
- NCIT_C49357 isDefinedBy ncit.owl @default.
- NCIT_C49357 label "EPHX1 wt Allele" @default.
- NCIT_C49357 subClassOf NCIT_C16612 @default.
- NCIT_C49357 subClassOf NCIT_C21281 @default.
- NCIT_C49357 subClassOf NCIT_C25804 @default.
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