Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion> ?p ?o ?g. }
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- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion type Assertion NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_head.
- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_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." NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_provenance.
- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion evidence source_evidence_literature NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_provenance.
- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion SIO_000772 14570709 NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_provenance.
- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion wasDerivedFrom befree-20150227 NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_provenance.
- NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_assertion wasGeneratedBy ECO_0000203 NP578349.RAJoX8wyfypJvgW8e0vsa-kHsHng8pVDXarLs6HV4QJUY130_provenance.