Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion> ?p ?o ?g. }
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- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion type Assertion NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_head.
- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion evidence source_evidence_literature NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion SIO_000772 21882291 NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion wasDerivedFrom befree-20140225 NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_assertion wasGeneratedBy ECO_0000203 NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.