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Q48273157-D82B13EE-637E-47BF-AB18-54602176F38E
Q48273157-D82B13EE-637E-47BF-AB18-54602176F38E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48273157-D82B13EE-637E-47BF-AB18-54602176F38E
Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.
P2860
Q48273157-D82B13EE-637E-47BF-AB18-54602176F38E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48273157-D82B13EE-637E-47BF-AB18-54602176F38E
rank
NormalRank
type
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Statement
wasDerivedFrom
3d60844cc233d371f410b9514fe4450000cd24a8
P2860
The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.