Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion> ?p ?o ?g. }
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- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion type Assertion NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_head.
- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_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." NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_provenance.
- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion evidence source_evidence_literature NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_provenance.
- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion SIO_000772 14570709 NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_provenance.
- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion wasDerivedFrom befree-20150227 NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_provenance.
- NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_assertion wasGeneratedBy ECO_0000203 NP766688.RASF-HH9I8pW3-PRbZ4RWmQCPHh_-rTC4Hn2pYGPY2eIQ130_provenance.