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Q36674906-2767C406-449F-4778-B397-9A6E066B5611
Q36674906-2767C406-449F-4778-B397-9A6E066B5611
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http://www.wikidata.org/entity/statement/Q36674906-2767C406-449F-4778-B397-9A6E066B5611
Identification of OCTN2 variants and their association with phenotypes of Crohn's disease in a Korean population.
P2860
Q36674906-2767C406-449F-4778-B397-9A6E066B5611
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36674906-2767C406-449F-4778-B397-9A6E066B5611
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wasDerivedFrom
cf493e243e4025fc99dde53e34d663ec95810916
P2860
A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease