Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_assertion description "[Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_assertion evidence source_evidence_curated NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_assertion SIO_000772 2215617 NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_assertion wasDerivedFrom uniprot-2016 NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_assertion wasGeneratedBy ECO_0000218 NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6877.RAwF12Dvc_kSDEl-nNGdh3aK15y6NZnRV2d8Kf0SXuwDk130_provenance.