Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion type Assertion NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_head.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_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." NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion evidence source_evidence_literature NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion SIO_000772 10826984 NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion wasDerivedFrom befree-20140225 NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.
- NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion wasGeneratedBy ECO_0000203 NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.