Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_assertion wasGeneratedBy ECO_0000203 NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_assertion wasDerivedFrom befree-20140225 NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_assertion SIO_000772 9719147 NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_assertion evidence source_evidence_literature NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_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." NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP556715.RAhwqUQ6qUsoabi_9IjM5oOEneY47ayAly5F68Lkw_0S0130_provenance.