Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion description "[A variant located at the 3' UTR of the FGF2 gene (rs6820411) was highly associated with atrophic AMD, and the functional SNP rs3112831 at ABCA4 showed a marginal association with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion evidence source_evidence_literature NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion SIO_000772 21106043 NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion wasDerivedFrom befree-20150227 NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion wasGeneratedBy ECO_0000203 NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.