Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_assertion description "[SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_assertion evidence source_evidence_literature NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_assertion SIO_000772 15944908 NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_assertion wasDerivedFrom befree-2016 NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_assertion wasGeneratedBy ECO_0000203 NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.
- befree-2016 importedOn "2016-02-19" NP498587.RARrdv_HZKdGSEMikpuhvJxF53XgBu8FkMKl3dblVpZ8A130_provenance.