Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion> ?p ?o ?g. }
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- NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_assertion type Assertion NP4186.RAWi7aQIDV8FED0PnNpOtdCO5cdcJI1CTUiDOs_NPZcJ0130_head.
- 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.