Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_assertion description "[On the other hand, two human genes that cause lissencephaly (LIS1, DCX) encode proteins that have recently been implicated as regulators or microtubule dynamics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_assertion evidence source_evidence_literature NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_assertion SIO_000772 10899795 NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_assertion wasDerivedFrom befree-2016 NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_assertion wasGeneratedBy ECO_0000203 NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP289363.RAnUFe9OyvZB7e3fXln-1zny7oQKZtiFsP1Z6ffsEe34Y130_provenance.