Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_assertion description "[The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_assertion evidence source_evidence_literature NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_assertion SIO_000772 22558177 NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_assertion wasDerivedFrom befree-2016 NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_assertion wasGeneratedBy ECO_0000203 NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.
- befree-2016 importedOn "2016-02-19" NP979679.RAXmCU9vI14X2tC4L-EoEekW0o7FnVWfxIm6ZJMjjwaiY130_provenance.