Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion> ?p ?o ?g. }
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- NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_assertion type Assertion NP137315.RAsJYu50G3j7mipsEjK6bBy4IEWqsB5esjfHX-T3a-WdI130_head.
- 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.