Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_assertion description "[Heterozygous mutations in ELOVL4, the gene encoding one of the elongases, are known to cause macular degeneration in humans and retinal abnormalities in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_assertion evidence source_evidence_literature NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_assertion SIO_000772 22100072 NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_assertion wasDerivedFrom befree-20150227 NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_assertion wasGeneratedBy ECO_0000203 NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP718600.RA3sk8Wbue57b1nmWGiOj05il_HAMoAPJyzh1ILBcp5TQ130_provenance.