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- source_evidence_literature type ECO_0000212 NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion evidence source_evidence_literature NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion SIO_000772 7650604 NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion wasDerivedFrom befree-20150227 NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion wasGeneratedBy ECO_0000203 NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.