Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion> ?p ?o ?g. }
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- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion type Assertion NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_head.
- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion description "[However, genetic heterogeneity occurs in MH and a mutation in a second gene (CACLN1A3), encoding the alpha1-subunit of the dihydropyridine (DHP) channel, has recently been found in a large MH French family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion evidence source_evidence_literature NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion SIO_000772 11216663 NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion wasDerivedFrom befree-20140225 NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_assertion wasGeneratedBy ECO_0000203 NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.