Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_assertion description "[Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_assertion evidence source_evidence_literature NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_assertion SIO_000772 22833210 NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_assertion wasDerivedFrom befree-20140225 NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_assertion wasGeneratedBy ECO_0000203 NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP457412.RAUwr41xohNokV1bhPcoPlL-MIb1DbyI9P0ssKUbPTO0c130_provenance.