Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_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." NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_assertion evidence source_evidence_literature NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_assertion SIO_000772 21106043 NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_assertion wasDerivedFrom befree-20140225 NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_assertion wasGeneratedBy ECO_0000203 NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.