Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_assertion description "[Ten eyes of 5 patients diagnosed with CSNB2 (4 X-linked recessive, 1 autosomal recessive) and 6 eyes of 3 patients with RP (2 autosomal dominant, 1 autosomal recessive) were evaluated with spectral-domain optical coherence tomography (SD OCT) and fundus autofluorescence (FAF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_assertion evidence source_evidence_literature NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_assertion SIO_000772 21920492 NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_assertion wasDerivedFrom befree-20140225 NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_assertion wasGeneratedBy ECO_0000203 NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP386058.RAm3mKjpxFndUjQQQVsDWNb-JbwUbh2TY7rCzYghPf5iQ130_provenance.