Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_assertion wasGeneratedBy ECO_0000203 NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_assertion wasDerivedFrom befree-20150227 NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_assertion SIO_000772 9719147 NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_assertion evidence source_evidence_literature NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.
- NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_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." NP872527.RA24-k3U_RO1YfeLDwbZ-MOWom_SSI6T9R-Rh2lMTovr8130_provenance.