Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_assertion description "[Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_assertion evidence source_evidence_literature NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_assertion SIO_000772 19818506 NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_assertion wasDerivedFrom befree-20150227 NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_assertion wasGeneratedBy ECO_0000203 NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.
- befree-20150227 importedOn "2015-02-27" NP805193.RA3oXjKyPXCBDqZmyCW6szZtNssi7QOR_XMH6uwxEVX18130_provenance.