Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_assertion description "[Polymorphisms in PDE9A and PDE11A were found to be associated with the diagnosis of MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_assertion evidence source_evidence_literature NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_assertion SIO_000772 17008408 NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_assertion wasDerivedFrom befree-2016 NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_assertion wasGeneratedBy ECO_0000203 NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.
- befree-2016 importedOn "2016-02-19" NP571842.RAnQXCLLmRunji6WmV5je7Vywcgv1hP3wflslOSjlhS7g130_provenance.