Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_assertion description "[Inherited factors account for around one third of all colorectal cancers (CRCs) and include rare high penetrance mutations in APC, MSH2, MSH6, and POLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_assertion evidence source_evidence_literature NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_assertion SIO_000772 23585368 NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_assertion wasDerivedFrom befree-2016 NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_assertion wasGeneratedBy ECO_0000203 NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1069178.RASJ5XVP-MGWODw5q3ziziYoYgcHnQ0_Es-JcnHBhJq3I130_provenance.