Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion> ?p ?o ?g. }
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- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion type Assertion NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_head.
- 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.
- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion evidence source_evidence_literature NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_provenance.
- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion SIO_000772 16464983 NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_provenance.
- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion wasDerivedFrom befree-2016 NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_provenance.
- NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_assertion wasGeneratedBy ECO_0000203 NP534975.RAEZuHiMEy3tgwjp2BQ4_MhXjG3tM6KLRtuZP4U57ldak130_provenance.