Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_assertion description "[Our data show that a heterozygous mutation in EAAT1 can lead to decreased glutamate uptake, which can contribute to neuronal hyperexcitability to cause seizures, hemiplegia, and episodic ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_assertion evidence source_evidence_literature NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_assertion SIO_000772 16116111 NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_assertion wasDerivedFrom lhgdn-20090331 NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_assertion wasGeneratedBy ECO_0000203 NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212708.RA8pX9VNDWg2mcFUG0JAtOQkrrOg3hI28gt_MXGPmPRkw130_provenance.