Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_assertion description "[The first two cases demonstrate that mutations in HNF1A (MODY3) can cause hyperinsulinism early in life and diabetes later, similar to the phenotype recently reported for HNF4A (MODY1) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_assertion evidence source_evidence_literature NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_assertion SIO_000772 22802087 NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_assertion wasDerivedFrom befree-2016 NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_assertion wasGeneratedBy ECO_0000203 NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.
- befree-2016 importedOn "2016-02-19" NP998038.RAc-nfSQxcvenPVC86_JFdy667D6hJMggLZGGF7-o4sR8130_provenance.