Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_assertion description "[Genetic interaction between the combined mild alleles of monogenic epilepsy genes KCNQ2 and SCN2A1 results in severe epilepsy in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_assertion evidence source_evidence_literature NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_assertion SIO_000772 16464983 NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_assertion wasDerivedFrom lhgdn-20090331 NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_assertion wasGeneratedBy ECO_0000203 NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP190153.RA6pvIQR0PDB_kg_qb7w1zovfKbQjU1zl5yN3WvK84jJc130_provenance.