Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion> ?p ?o ?g. }
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- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion type Assertion NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_head.
- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.
- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion evidence source_evidence_literature NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.
- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion SIO_000772 18264947 NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.
- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion wasDerivedFrom gad-20130706 NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.
- NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion wasGeneratedBy ECO_0000203 NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.