Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_assertion description "[Patients with CSNB2 had specific findings on SD OCT and FAF that were distinct from those found in RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_assertion evidence source_evidence_literature NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_assertion SIO_000772 21920492 NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_assertion wasDerivedFrom befree-20140225 NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_assertion wasGeneratedBy ECO_0000203 NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP238759.RAfSmSp59It6oYGOvmm9WZEHXwPt4wipHPUWubscSlQ-k130_provenance.