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Q35361558-2077A787-5526-4309-AA2F-FC51BBE6789F
Q35361558-2077A787-5526-4309-AA2F-FC51BBE6789F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35361558-2077A787-5526-4309-AA2F-FC51BBE6789F
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome
P698
Q35361558-2077A787-5526-4309-AA2F-FC51BBE6789F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35361558-2077A787-5526-4309-AA2F-FC51BBE6789F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ffbec7288ebe5c6c4b724646feb8429b2cd96ab9
P698
25412741
http://www.w3.org/2001/XMLSchema#string