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Q37693348-2C27E497-EB1A-4280-9157-0B17E318DA7F
Q37693348-2C27E497-EB1A-4280-9157-0B17E318DA7F
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http://www.wikidata.org/entity/statement/Q37693348-2C27E497-EB1A-4280-9157-0B17E318DA7F
Rare variants in NR2F2 cause congenital heart defects in humans.
P2860
Q37693348-2C27E497-EB1A-4280-9157-0B17E318DA7F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37693348-2C27E497-EB1A-4280-9157-0B17E318DA7F
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wasDerivedFrom
96e7e20394f9289a4226ec10eef90ba416403034
P2860
Functional domains of the human orphan receptor ARP-1/COUP-TFII involved in active repression and transrepression