Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_assertion description "[The disease complex medullary cystic disease/familial juvenile hyperuricemic nephropathy (MCKD/FJHN) is characterized by alteration of urinary concentrating ability, frequent hyperuricemia, tubulo-interstitial fibrosis, cysts at the cortico-medullary junction and renal failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_assertion evidence source_evidence_literature NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_assertion SIO_000772 14570709 NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_assertion wasDerivedFrom befree-2016 NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_assertion wasGeneratedBy ECO_0000203 NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.
- befree-2016 importedOn "2016-02-19" NP417688.RAAVc5c3tcZqPvpQRQxo8t84Ze3AJb0wtOFIV9XoCg0HU130_provenance.