Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- 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." 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.
- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_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." NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_provenance.