Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_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." NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_assertion evidence source_evidence_literature NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_assertion SIO_000772 19818506 NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_assertion wasDerivedFrom befree-20150227 NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_assertion wasGeneratedBy ECO_0000203 NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.