Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion evidence source_evidence_literature NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion SIO_000772 19818506 NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion wasDerivedFrom befree-20140225 NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion wasGeneratedBy ECO_0000203 NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.