Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_assertion description "[The CHEK2 1100delC was not significantly increased in Swedish colorectal cancer patients, however, in order to determine the role of the variant in colorectal cancer families with the history of breast cancer a larger sample size is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_assertion evidence source_evidence_literature NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_assertion SIO_000772 17214356 NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_assertion wasDerivedFrom befree-2016 NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_assertion wasGeneratedBy ECO_0000203 NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.
- befree-2016 importedOn "2016-02-19" NP588084.RAnzg35IuUrrihHs66QokMkDtV5mZ46FEkNMzVh18n0Tk130_provenance.