Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion> ?p ?o ?g. }
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- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion type Assertion NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_head.
- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion wasGeneratedBy ECO_0000203 NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_provenance.
- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion wasDerivedFrom befree-20140225 NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_provenance.
- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion SIO_000772 9719147 NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_provenance.
- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion evidence source_evidence_literature NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_provenance.
- NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_assertion description "[Autosomal dominant medullary cystic kidney disease (ADMCKD; synonym: medullary cystic disease, MCD) is an autosomal dominant kidney disorder, sharing morphological and clinical features with recessive juvenile nephronophthisis (NPH), such as reduced urinary concentration ability and multiple renal cysts at the corticomedullary junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334264.RAny72wmCaPkoC_ypSP6FkIfPuIAL466Uu56ucCMTe1C4130_provenance.