Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion description "[To examine the phenotypes of 8 patients with evidence of cone dysfunction and normal color vision (characteristic features of both oligocone trichromacy and bradyopsia), and subsequently to screen RGS9 and R9AP for disease-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion evidence source_evidence_literature NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion SIO_000772 19818506 NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion wasDerivedFrom befree-20140225 NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_assertion wasGeneratedBy ECO_0000203 NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220439.RAIpX4ztO1xZNQ1lBmCGL9cLiD5heqLEueZZSJz0WjdWg130_provenance.