Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_assertion wasGeneratedBy ECO_0000203 NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_assertion wasDerivedFrom befree-20140225 NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_assertion SIO_000772 9719147 NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_assertion evidence source_evidence_literature NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_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." NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP592373.RANEV26G3VPQuUZCjoqm7qgWRWyah3hx5T6zYOTs8II7Q130_provenance.