Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_assertion description "[However, unlike two other alleles previously associated with Best disease, cotransfection with wild-type bestrophin-1 did not impair the formation of active wild-type bestrophin-1 channels, consistent with the recessive nature of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_assertion evidence source_evidence_curated NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_assertion SIO_000772 18179881 NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_assertion wasDerivedFrom uniprot-2016 NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_assertion wasGeneratedBy ECO_0000218 NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5226.RAmlG_2-HPzf9thv6PEFwkevuauhMyH13quANgrot2-ug130_provenance.