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- source_evidence_literature type ECO_0000212 NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.