Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion> ?p ?o ?g. }
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- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion type Assertion NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_head.
- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion description "[Hyperkalaemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotonia are three autosomal dominant skeletal muscle disorders linked to the SCN4A gene encoding the alpha-subunit of the human voltage-sensitive sodium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_provenance.
- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion evidence source_evidence_literature NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_provenance.
- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion SIO_000772 10366610 NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_provenance.
- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion wasDerivedFrom befree-2016 NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_provenance.
- NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_assertion wasGeneratedBy ECO_0000203 NP254878.RAxiAEdt0uHS3NkTMYmtXZBIN2SNsMQtx1jq-BXTdWe84130_provenance.