Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion description "[We previously identified variants at the CSF1, OPTN and TNFRSF11A loci as risk factors for PDB by genome-wide association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion evidence source_evidence_literature NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion SIO_000772 21623375 NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion wasDerivedFrom gad-20130706 NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_assertion wasGeneratedBy ECO_0000203 NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96100.RAptwkKdEJVfVugdEwXsyIzZiRMXt8SVsvtLk6GGdYasQ130_provenance.