Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_assertion wasGeneratedBy ECO_0000203 NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_assertion wasDerivedFrom befree-20150227 NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_assertion SIO_000772 9719147 NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_assertion evidence source_evidence_literature NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.
- NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_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." NP578685.RAMM9qutdeq8YuswQB8KGsJeyoZoI_oBtVesg_Zi8JKqs130_provenance.