Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_assertion description "[A yet unresolved issue involves the relationship between early myoclonic encephalopathy (EME-ErbB4 mutations) versus the EIEE spectrum of disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_assertion evidence source_evidence_literature NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_assertion SIO_000772 21967765 NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_assertion wasDerivedFrom befree-20150227 NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_assertion wasGeneratedBy ECO_0000203 NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381116.RAoqYWf69p5cAZ5S8dWtesIN1G0c3m-4hJEHBhoDTu6-s130_provenance.