Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion> ?p ?o ?g. }
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- NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_assertion type Assertion NP424390.RAPy4gZSrFyg4_NUJDDCs5PUTke0UtqLE1iJUBpe0bWCk130_head.
- 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.