Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion> ?p ?o ?g. }
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- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion type Assertion NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_head.
- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion wasGeneratedBy ECO_0000203 NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion wasDerivedFrom befree-20140225 NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion SIO_000772 9719147 NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_assertion evidence source_evidence_literature NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_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." NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.