Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_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." NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_assertion evidence source_evidence_literature NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_assertion SIO_000772 16464983 NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_assertion wasDerivedFrom lhgdn-20090331 NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_assertion wasGeneratedBy ECO_0000203 NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP126969.RAt5yD65oXcM2gka38TNbrD8Gr7L9EQAHo3qcpwHQ2ogY130_provenance.