Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion type Assertion NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_head.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion wasGeneratedBy ECO_0000203 NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_provenance.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion wasDerivedFrom befree-20140225 NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_provenance.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion SIO_000772 23446743 NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_provenance.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion evidence source_evidence_literature NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_provenance.
- NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_assertion description "[In previous studies, we identified a loss-of-function mutation in the Cyba gene as the primary cause of hereditary eosinophilia in the Matsumoto Eosinophilia Shinshu (MES) rat strain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243213.RAiUj7-Ep0rc3hkhz35teAXOpeIRSTZurQz32rOEPUI3A130_provenance.