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- source_evidence_literature type ECO_0000212 NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_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." NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_assertion evidence source_evidence_literature NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_assertion SIO_000772 20164212 NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_assertion wasDerivedFrom befree-2016 NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_assertion wasGeneratedBy ECO_0000203 NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP794442.RAh65h-QB4ZV-xS1qvNQTEQkXALicG30lizXCfBgyQEJQ130_provenance.