Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion evidence source_evidence_literature NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion SIO_000772 23429546 NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion wasDerivedFrom befree-2016 NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion wasGeneratedBy ECO_0000203 NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.