wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Triples
Insights
Schema
BETA
Class frequency
Class hierarchy
SPARQL
Graphs
1
Q38308028-14E6EC20-3FD2-4CD4-BE26-27967381A7DF
Q38308028-14E6EC20-3FD2-4CD4-BE26-27967381A7DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-14E6EC20-3FD2-4CD4-BE26-27967381A7DF
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P2860
Q38308028-14E6EC20-3FD2-4CD4-BE26-27967381A7DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-14E6EC20-3FD2-4CD4-BE26-27967381A7DF
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2fd4d693cd71e5da7aa3d5ff043f5adcf713aecc
P2860
Rare copy number variants contribute to congenital left-sided heart disease.