Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP394062.RAYAIsm5hme81r0QbUiTSqozm2-fGGqfIbKRL9r4aqw2g#assertion> ?p ?o ?g. }
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- 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." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 21106043 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.