Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion type Assertion NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_head.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_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." NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion evidence source_evidence_literature NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion SIO_000772 10826984 NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion wasDerivedFrom befree-2016 NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion wasGeneratedBy ECO_0000203 NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.