Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_assertion wasGeneratedBy ECO_0000218 NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_assertion wasDerivedFrom ctd_human-2016 NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_assertion SIO_000772 15579781 NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_assertion evidence source_evidence_curated NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.
- NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_assertion description "[Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14841.RAQ6vmBOLg-I8BUrq3gtq1WTqAQfeTD-wJg4J8MgSr0nA130_provenance.