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Q51318832-7F70E7C5-2F61-46C2-A0EE-E2C57D230536
Q51318832-7F70E7C5-2F61-46C2-A0EE-E2C57D230536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51318832-7F70E7C5-2F61-46C2-A0EE-E2C57D230536
Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features.
P2860
Q51318832-7F70E7C5-2F61-46C2-A0EE-E2C57D230536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51318832-7F70E7C5-2F61-46C2-A0EE-E2C57D230536
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
3a12216639de658a86f18c793496bce499d59aaf
P2860
Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta