Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_assertion description "[A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_assertion evidence source_evidence_literature NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_assertion SIO_000772 23246292 NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_assertion wasDerivedFrom befree-20140225 NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_assertion wasGeneratedBy ECO_0000203 NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP897789.RA-c2ly9yjkHA2y1fMmwcjGn04yMmV69ELRrtpqYc0wCM130_provenance.