Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_assertion description "[Recently, the 1100delC variant of cell cycle checkpoint kinase 2 (CHEK2) has been reported to confer a colorectal cancer risk in hereditary non-polyposis-colorectal cancer (HNPCC) and HNPCC-related families in the Netherlands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_assertion evidence source_evidence_literature NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_assertion SIO_000772 19876921 NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_assertion wasDerivedFrom befree-20140225 NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_assertion wasGeneratedBy ECO_0000203 NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782573.RAYHlmtJ_lWJmWD9VfXADeZRuprvDi0ssFWrrHfEwW-5k130_provenance.