Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.