Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion> ?p ?o ?g. }
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- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion type Assertion NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_head.
- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion description "[The two autosomal dominantly inherited neurological diseases: familial hemiplegic migraine type 2 (FHM2) and familial rapid-onset of dystonia-parkinsonism (Familial RDP) are caused by in vivo mutations of specific alpha subunits of the sodium-potassium pump (Na(+)/K(+)-ATPase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion evidence source_evidence_literature NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion SIO_000772 22067897 NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion wasDerivedFrom befree-20150227 NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_assertion wasGeneratedBy ECO_0000203 NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.