Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_assertion description "[The frequency of the delA750 mutation was significantly increased in idiopathic generalized epilepsy (7.9%) compared to that in the controls (5.5%; P = 0.016, one-sided; OR = 1.52; 95%-CI: 1.05-2.21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_assertion evidence source_evidence_literature NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_assertion SIO_000772 16958040 NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_assertion wasDerivedFrom lhgdn-20090331 NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_assertion wasGeneratedBy ECO_0000203 NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP191952.RA2ftAXscRdn1I91veCL-q1qo2r07J94fC0Vf1nwfz1Xo130_provenance.