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- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_assertion type Assertion NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_head.
- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_assertion wasGeneratedBy ECO_0000203 NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_provenance.
- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_assertion wasDerivedFrom befree-20150227 NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_provenance.
- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_assertion SIO_000772 9719147 NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_provenance.
- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_assertion evidence source_evidence_literature NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_provenance.
- NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_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." NP872512.RA99BwfUTzhlFoJrszQonTo-KB2BEjOhNujpAh01kG4mk130_provenance.