Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_assertion description "[Therefore, as a supplement to ERG and genetic testing, we advocate the use of FAF and SD OCT in the examination of patients with CSNB2 and RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_assertion evidence source_evidence_literature NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_assertion SIO_000772 21920492 NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_assertion wasDerivedFrom befree-20140225 NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_assertion wasGeneratedBy ECO_0000203 NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213655.RAXkSUIYhrCzGOzXHhC6UYjTLVhSliW8lrfW7a8BVJlt0130_provenance.