Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_assertion wasGeneratedBy ECO_0000203 NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_assertion wasDerivedFrom befree-20140225 NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_assertion SIO_000772 24207121 NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_assertion evidence source_evidence_literature NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_assertion description "[A third CHD2 mutation was identified in an epileptic proband of a second (stage 2) cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726380.RAO18sHLcDK0Y_WBTWuoH0-5oe2dsCn2Xm2qtF0o0RwJY130_provenance.