Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion wasGeneratedBy ECO_0000203 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion wasDerivedFrom befree-20140225 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion SIO_000772 17056636 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion evidence source_evidence_literature NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion description "[Remarkably, our cohort of individuals with KRAS mutations showed a high clinical variability, ranging from Noonan syndrome to CFC, and also included two patients who met the clinical criteria of Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.