Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_assertion description "[GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_assertion evidence source_evidence_literature NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_assertion SIO_000772 23933820 NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_assertion wasDerivedFrom befree-2016 NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_assertion wasGeneratedBy ECO_0000203 NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1101114.RA3QN2EA9NR63auw6s91lG8_zu8E5o-RO_svgN8M3Vun8130_provenance.