Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion description "[Due to the unique role of 11-cis retinol dehydrogenase in the generation of visual pigments, it is a candidate gene for involvement in hereditary eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion evidence source_evidence_literature NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion SIO_000772 8884265 NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion wasDerivedFrom befree-20140225 NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_assertion wasGeneratedBy ECO_0000203 NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP661483.RA86z_OLCnXeEYivHKB3hw-ehh3By4Bq7i-oU474z_JGs130_provenance.