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Q42592424-51DE4BE5-0EBA-4DAF-850C-0AB33B32BE56
Q42592424-51DE4BE5-0EBA-4DAF-850C-0AB33B32BE56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42592424-51DE4BE5-0EBA-4DAF-850C-0AB33B32BE56
Endothelial chromosome 13 deletion in congenital heart disease-associated pulmonary arterial hypertension dysregulates SMAD9 signaling.
P921
Q42592424-51DE4BE5-0EBA-4DAF-850C-0AB33B32BE56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42592424-51DE4BE5-0EBA-4DAF-850C-0AB33B32BE56
rank
NormalRank
type
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Statement
P921
birth defect