Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion description "[A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion evidence source_evidence_literature NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion SIO_000772 18755274 NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion wasDerivedFrom befree-20140225 NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion wasGeneratedBy ECO_0000203 NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_provenance.