Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_assertion wasGeneratedBy ECO_0000203 NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_assertion wasDerivedFrom befree-20150227 NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_assertion SIO_000772 19139306 NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_assertion evidence source_evidence_literature NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.
- NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_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." NP695383.RAcPXOAKrtjXg7MIPL6udz77sUpTSfnDwQLi9xo-BZufg130_provenance.