Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP755028.RAD5dXT12h7rWEwePIkpybkoQxeODRgTyxrk9FclVHRIc130_provenance.