Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_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." NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_assertion evidence source_evidence_literature NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_assertion SIO_000772 22067897 NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_assertion wasDerivedFrom befree-2016 NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_assertion wasGeneratedBy ECO_0000203 NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.
- befree-2016 importedOn "2016-02-19" NP937161.RAvldIrR6L4mbEDFaUuoITMNFs1q7lBFQJfCqiyymvPco130_provenance.