Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP686715.RAm3tyhrYVJ7RO9JVJx92M428ht9N1ASXJOM02aSPwReI130_provenance.