Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_assertion description "[The allelic and genotypic frequencies of three LOXL1 variants (rs1048661, rs3825942, and rs2165241) were determined in 68 consecutive Japanese patients with CRVO [15 with exfoliation syndrome (EX+) and 53 without exfoliation syndrome (EX-)] and 90 control patients with cataract without EX (CT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_assertion evidence source_evidence_literature NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_assertion SIO_000772 25130441 NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_assertion wasDerivedFrom befree-2016 NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_assertion wasGeneratedBy ECO_0000203 NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211369.RAnooU3QMZFYHvtRMCSM6MkLglUEZv2xshPQw1MIPAba0130_provenance.