Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_assertion wasGeneratedBy ECO_0000203 NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_assertion wasDerivedFrom befree-20150227 NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_assertion SIO_000772 12234310 NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_assertion evidence source_evidence_literature NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.
- NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_assertion description "[Autosomal-dominant medullary cystic kidney disease (ADMCKD), a hereditary chronic interstitial nephropathy, recently attracted attention because of the cloning or mapping of certain gene loci, namely NPHP1, NPHP2 and NPHP3 for familial juvenile nephronophthisis (NPH) and MCKD1 and MCKD2 for the adult form of medullary cystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886260.RAsnMCRjcbpvRmoEQ2IVIP0XKX-A7iA4HMsbsRnCrzObY130_provenance.