Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_assertion description "[We conclude that mutations in the EFHC1 gene may underlie different types of epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_assertion evidence source_evidence_literature NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_assertion SIO_000772 17159113 NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_assertion wasDerivedFrom befree-20150227 NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_assertion wasGeneratedBy ECO_0000203 NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964416.RAFWaPlkMvXqKiX5mR7J5NerYLH2NsMkLDByemOV8gVWw130_provenance.