Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion> ?p ?o ?g. }
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- NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_assertion type Assertion NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_head.
- 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.