Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_assertion description "[In contrast, when the inheritance is complex, the epileptic phenotype is determined by several minor genetic defects that are much more difficult to discover.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_assertion evidence source_evidence_literature NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_assertion SIO_000772 18754913 NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_assertion wasDerivedFrom befree-20150227 NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_assertion wasGeneratedBy ECO_0000203 NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP787892.RA9WxX46DeuOVWCp7FksBsLhvHZDIzEgZszM06-8Wj8dk130_provenance.