Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion> ?p ?o ?g. }
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- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion type Assertion NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_head.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion evidence source_evidence_literature NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion SIO_000772 16754686 NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion wasDerivedFrom befree-2016 NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion wasGeneratedBy ECO_0000203 NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.