Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_assertion description "[Thus, we identified CUBN rs7918972 as a novel risk variant for renal function loss in two independent settings: ESRD in native kidneys and GF in transplanted kidneys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_assertion evidence source_evidence_literature NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_assertion SIO_000772 22574174 NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_assertion wasDerivedFrom befree-20150227 NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_assertion wasGeneratedBy ECO_0000203 NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788398.RAp8PgtscqEZdt6fovBjpZpWwUmarWoOHQVL3vNp_EBbI130_provenance.