Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_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." NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_assertion evidence source_evidence_literature NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_assertion SIO_000772 14570709 NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_assertion wasDerivedFrom befree-2016 NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_assertion wasGeneratedBy ECO_0000203 NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.
- befree-2016 importedOn "2016-02-19" NP417691.RA3OMbEJYUMijPn5I-Vp2P0Zcp3URLzsTc0X9U_j5mDpE130_provenance.