Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion description "[The genetic interaction between Scn2a and Kcnq2 demonstrates that combinations of mild alleles of monogenic epilepsy genes can result in severe disease and provides a model for complex inheritance of human epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion evidence source_evidence_literature NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion SIO_000772 16464983 NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion wasDerivedFrom befree-2016 NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion wasGeneratedBy ECO_0000203 NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.
- befree-2016 importedOn "2016-02-19" NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_provenance.