Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion description "[Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause 'cone dystrophy with supernormal rod electroretinogram' in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion evidence source_evidence_curated NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion SIO_000772 16909397 NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion wasDerivedFrom uniprot-20150221 NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion wasGeneratedBy ECO_0000218 NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_provenance.