Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_assertion wasGeneratedBy ECO_0000203 NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_assertion wasDerivedFrom befree-20140225 NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_assertion SIO_000772 16505158 NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_assertion evidence source_evidence_literature NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_assertion description "[Considering all features, CORDX3 is more similar to other X chromosomal cone-rod dystrophies than to CSNB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP324032.RA6N1WUazmAFO9BwUPIvp_tWApb1Y5eh6669KF0FYNhRM130_provenance.