Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_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." NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion evidence source_evidence_curated NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion SIO_000772 16909397 NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion wasDerivedFrom uniprot-2016 NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion wasGeneratedBy ECO_0000218 NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_provenance.