Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_assertion description "[Array CGH was used to identify recurrent copy number alterations (RCNA) characteristic of either BRCA1-related or sporadic ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_assertion evidence source_evidence_literature NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_assertion SIO_000772 19802895 NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_assertion wasDerivedFrom befree-2016 NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_assertion wasGeneratedBy ECO_0000203 NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.
- befree-2016 importedOn "2016-02-19" NP767307.RAmL7lS17qjQhGy4gfd-Ila1W-1ZTgScrpZv9YHOht9us130_provenance.