Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_assertion description "[Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_assertion evidence source_evidence_curated NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_assertion SIO_000772 10447650 NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_assertion wasDerivedFrom uniprot-20130724 NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_assertion wasGeneratedBy ECO_0000218 NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4225.RAnD4BWya9DV1FBi3SW71RGkdXCyRGWBVs2y3un-9k3FA130_provenance.