Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_assertion description "[AMD is a complex disorder caused by genetic and environmental factors in which single nucleotide polymorphisms (SNPs) in the genes CFH and LOC387715/HTRA1/ARMS2 have prognostic importance for progression to advanced AMD (with visual loss).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_assertion evidence source_evidence_literature NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_assertion SIO_000772 19015224 NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_assertion wasDerivedFrom befree-20150227 NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_assertion wasGeneratedBy ECO_0000203 NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446646.RAtIG4aOe7O94OF24Xh6U5n_7nBWdirJh3y7-rFOaunGg130_provenance.