Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_assertion type Assertion NP4652.RAKVMngfDpYg5rylWMRVNaSI3jiLli61tt3dRUcrQCMsc130_head.
- 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.