Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_assertion description "[Lissencephaly caused by LIS1 or DCX mutation frequently results in West syndrome, while lissencephaly due to ARX mutation is associated with the most severe form of epilepsy but never results in West syndrome nor infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_assertion evidence source_evidence_literature NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_assertion SIO_000772 16806828 NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_assertion wasDerivedFrom befree-20150227 NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_assertion wasGeneratedBy ECO_0000203 NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP350652.RAjX6H74GGegYUAzHWqVlUoou3JFQVlxG9fSwtMqIUOdE130_provenance.