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Q37166261-1C8836E3-F463-43F1-B044-36A77042BFA7
Q37166261-1C8836E3-F463-43F1-B044-36A77042BFA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37166261-1C8836E3-F463-43F1-B044-36A77042BFA7
Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.
P2860
Q37166261-1C8836E3-F463-43F1-B044-36A77042BFA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37166261-1C8836E3-F463-43F1-B044-36A77042BFA7
rank
NormalRank
type
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Statement
wasDerivedFrom
2a5cd21b4a6e7dc2b947e8bfe5c9f306dce83c97
P2860
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism