Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion description "[Range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion evidence source_evidence_literature NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion SIO_000772 15277402 NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion wasDerivedFrom lhgdn-20090331 NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion wasGeneratedBy ECO_0000203 NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_provenance.