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- source_evidence_literature type ECO_0000212 NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion evidence source_evidence_literature NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion SIO_000772 10826984 NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion wasDerivedFrom befree-20150227 NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion wasGeneratedBy ECO_0000203 NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
- befree-20150227 importedOn "2015-02-27" NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.