Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- befree-2016 importedOn "2016-02-19" NP588238.RADAWpvVIJoy9ZvVNwd270hMxCd0fYy9uqnFt8AJ4OHUo130_provenance.
- 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.