Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP390886.RAMMKq2T2kvvXSfsgOP_WbVHhEQXLIYvgojeJ77eOBrnE130_provenance.