Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_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." NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_assertion evidence source_evidence_literature NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_assertion SIO_000772 19818506 NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_assertion wasDerivedFrom befree-20140225 NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_assertion wasGeneratedBy ECO_0000203 NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.