Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_assertion description "[A novel Kcnq2 missense mutation V182M was identified by screening the offspring of ENU-treated males for reduced threshold to electrically evoked minimal clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_assertion evidence source_evidence_literature NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_assertion SIO_000772 16464983 NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_assertion wasDerivedFrom befree-2016 NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_assertion wasGeneratedBy ECO_0000203 NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.
- befree-2016 importedOn "2016-02-19" NP534978.RAHKqXvDyHLb7gpCuPr7pdG6SCKOscGi-MSAJkMuGqatc130_provenance.