Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion> ?p ?o ?g. }
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- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion type Assertion NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_head.
- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_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." NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_provenance.
- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion evidence source_evidence_literature NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_provenance.
- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion SIO_000772 22067897 NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_provenance.
- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion wasDerivedFrom befree-20140225 NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_provenance.
- NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_assertion wasGeneratedBy ECO_0000203 NP830828.RAJDwPIfmkRn2rAyhJhp133hb2Jh4mkO5qM6j7_p_l1bQ130_provenance.