Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion description "[SCN2A gene mutations are associated with inherited benign neonatal-infantile epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion evidence source_evidence_literature NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion SIO_000772 18479388 NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion wasDerivedFrom lhgdn-20090331 NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_assertion wasGeneratedBy ECO_0000203 NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP237765.RAiEBVACIvHQrj7Ml_aIuG8_-dKJB4biUUZFsHrUyb-X0130_provenance.