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- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion type Assertion NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_head.
- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_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." NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.
- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion evidence source_evidence_literature NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.
- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion SIO_000772 10826984 NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.
- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion wasDerivedFrom befree-2016 NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.
- NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion wasGeneratedBy ECO_0000203 NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.