Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion> ?p ?o ?g. }
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- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion type Assertion NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_head.
- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion wasGeneratedBy ECO_0000203 NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_provenance.
- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion wasDerivedFrom befree-20140225 NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_provenance.
- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion SIO_000772 9359047 NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_provenance.
- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion evidence source_evidence_literature NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_provenance.
- NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_assertion description "[Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755189.RAtMkpLYRPGSrOd_1V0AdHdObkbP5erXX3zLIgJjPeSNI130_provenance.