Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion wasGeneratedBy ECO_0000203 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion wasDerivedFrom befree-20150227 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion SIO_000772 24076603 NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion evidence source_evidence_literature NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.
- NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_assertion description "[These findings suggest that MAGEL2 is a new gene causing complex ASD and that MAGEL2 loss of function can contribute to several aspects of the PWS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912032.RA89pGErOaxz0kPlAFZxUqmzjEvrp1pVjs6qgiSLkuU2E130_provenance.