Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion evidence source_evidence_literature NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion SIO_000772 22833210 NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion wasDerivedFrom befree-20140225 NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion wasGeneratedBy ECO_0000203 NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.