Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion> ?p ?o ?g. }
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- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion type Assertion NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_head.
- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_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." NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.
- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion evidence source_evidence_literature NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.
- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion SIO_000772 21106043 NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.
- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion wasDerivedFrom befree-20140225 NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.
- NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_assertion wasGeneratedBy ECO_0000203 NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.