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Q36015009-3C6F41F7-CF2D-41B1-A91D-720FCD66CBA1
Q36015009-3C6F41F7-CF2D-41B1-A91D-720FCD66CBA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36015009-3C6F41F7-CF2D-41B1-A91D-720FCD66CBA1
Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kappaB activation.
P2860
Q36015009-3C6F41F7-CF2D-41B1-A91D-720FCD66CBA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36015009-3C6F41F7-CF2D-41B1-A91D-720FCD66CBA1
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Statement
wasDerivedFrom
f9adda2ca41c2f6a6e4225e47d483d130f81423a
P2860
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains