Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP786086.RAZtJ0x_GKCc-MriAF1rQPqNPLEtSMR6Y30FTKf8ih-X0130_provenance.