Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_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." NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_assertion evidence source_evidence_literature NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_assertion SIO_000772 16464983 NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_assertion wasDerivedFrom lhgdn-20090331 NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_assertion wasGeneratedBy ECO_0000203 NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215467.RASvAe3H36mqoxpdTqtWkAv9fnTxQrpfqW6KBOwC-LQwg130_provenance.