Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_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." NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_assertion evidence source_evidence_curated NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_assertion SIO_000772 14570709 NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_assertion wasDerivedFrom uniprot-2016 NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_assertion wasGeneratedBy ECO_0000218 NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3061.RALiG2M16wyHMOCfFeNZpBQ2kO-CMCiYl0iIPj4ZIv62s130_provenance.