Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_assertion description "[Glomerulopathy with fibronectin (FN) deposits (GFND) is an autosomal dominant disease with age-related penetrance, characterized by proteinuria, microscopic hematuria, hypertension, and massive glomerular deposits of FN that lead to end-stage renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_assertion evidence source_evidence_literature NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_assertion SIO_000772 18268355 NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_assertion wasDerivedFrom befree-20140225 NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_assertion wasGeneratedBy ECO_0000203 NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP764922.RAAVbsmVMyKcprL3FqRatxxzMZNIIxIS-7229odt0v0YQ130_provenance.