Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- befree-2016 importedOn "2016-02-19" NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_assertion wasGeneratedBy ECO_0000203 NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_assertion wasDerivedFrom befree-2016 NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_assertion SIO_000772 11723059 NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_assertion evidence source_evidence_literature NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.
- NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_assertion description "[Most cases of hyperinsulinism of infancy (HI) are caused by mutations in either the sulfonylurea receptor-1 (SUR1) or the inward rectifying K(+) channel Kir6.2, two subunits of the beta-cell ATP-sensitive K(+) channel (K(ATP) channel).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337486.RAsMH1NaGv8fkgzJEhFnfmWNulIMRfpEwgXk8biEIB6ug130_provenance.