Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion> ?p ?o ?g. }
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- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion type Assertion NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_head.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion wasGeneratedBy ECO_0000203 NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion wasDerivedFrom befree-2016 NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion SIO_000772 17216245 NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion evidence source_evidence_literature NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.