Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion> ?p ?o ?g. }
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- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion type Assertion NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_head.
- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion wasGeneratedBy ECO_0000218 NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_provenance.
- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion wasDerivedFrom uniprot-20130724 NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_provenance.
- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion SIO_000772 15161766 NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_provenance.
- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion evidence source_evidence_curated NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_provenance.
- NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_assertion description "[A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3299.RAKJtmzpb9dIHforyEU2CPRl8XydTnvoU6PT4Htp2EkVE130_provenance.