Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_assertion description "[K(ATP) channel mutations were most common (15%) followed by GLUD1 mutations causing hyperinsulinism with hyperammonemia (5.9%), and HNF4A mutations (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_assertion evidence source_evidence_literature NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_assertion SIO_000772 20164212 NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_assertion wasDerivedFrom befree-20140225 NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_assertion wasGeneratedBy ECO_0000203 NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919839.RAAx4XVMVAcQ8chAaRkgBZAi44hfAhaferUJMyzqOLy7o130_provenance.