Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_assertion description "[ARX is a crucial gene for the development of interneurons in the fetal brain, and a polyalanine expansion mutation of ARX causes mental retardation and seizures, including those of West syndrome, in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_assertion evidence source_evidence_literature NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_assertion SIO_000772 17668384 NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_assertion wasDerivedFrom befree-2016 NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_assertion wasGeneratedBy ECO_0000203 NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.
- befree-2016 importedOn "2016-02-19" NP622862.RAa5yIUc9ddmvWw1ZM5zX1CmazdsJlNZzPJOJXnn8SCPw130_provenance.