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- NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_assertion type Assertion NP534976.RAUJt3gxo8Rlt2P_98TumeJ7x0KcN-UKLnxricA_spujE130_head.
- 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.