Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_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." NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_assertion evidence source_evidence_literature NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_assertion SIO_000772 21106043 NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_assertion wasDerivedFrom befree-2016 NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_assertion wasGeneratedBy ECO_0000203 NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
- befree-2016 importedOn "2016-02-19" NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.