Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_assertion description "[Recently, mutations in RPGRIP were found to lead to the retinal dystrophy, Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_assertion evidence source_evidence_literature NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_assertion SIO_000772 12140192 NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_assertion wasDerivedFrom befree-20150227 NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_assertion wasGeneratedBy ECO_0000203 NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP927836.RAhqwbnMVQMojUcJMVQktEkR7bderTosb0uwvQpJb4DTo130_provenance.