Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- befree-2016 importedOn "2016-02-19" NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_assertion wasGeneratedBy ECO_0000203 NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_assertion wasDerivedFrom befree-2016 NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_assertion SIO_000772 19139306 NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_assertion evidence source_evidence_literature NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.
- NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_assertion description "[Recently, a mutation in the SLC1A3 gene encoding the glutamate transporter EAAT1 was identified in a patient with severe episodic and progressive ataxia, seizures, alternating hemiplegia, and migraine headache.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713673.RAhfN-Wnlxih6sNSOUX5aWXRy9ByX7mnljBuemojXhFVU130_provenance.