Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_assertion description "[Heterozygous inactivating mutations in the glucokinase gene (GCK) cause a mild form of diabetes (maturity-onset diabetes of the young [MODY]2), and activating mutations have been associated with a mild form of familial hyperinsulinemic hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_assertion evidence source_evidence_literature NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_assertion SIO_000772 15277402 NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_assertion wasDerivedFrom befree-20140225 NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_assertion wasGeneratedBy ECO_0000203 NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP363047.RAzWPnJfBJQjjFKvujTblgg5iqIf9vKl3rvFqAlsSI8W8130_provenance.