Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_assertion description "[Mutations in RDS can be associated with an intrafamilial variation in retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_assertion evidence source_evidence_literature NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_assertion SIO_000772 16916875 NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_assertion wasDerivedFrom befree-20140225 NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_assertion wasGeneratedBy ECO_0000203 NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP684843.RAEjobDd4FPb4xSuevAsxg4Tst-cASYNYtw1HRhf5qPEM130_provenance.