Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_assertion description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_assertion evidence source_evidence_literature NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_assertion SIO_000772 22738016 NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_assertion wasDerivedFrom befree-2016 NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_assertion wasGeneratedBy ECO_0000203 NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.
- befree-2016 importedOn "2016-02-19" NP993464.RAweF12edGqF-MwrZsMOvh3LC7npFBWKgbyqZCi-1TRDI130_provenance.