Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_assertion description "[We evaluated a series of European CRC patients and population controls to clarify whether EXO1 variants may indeed predispose to familial CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_assertion evidence source_evidence_literature NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_assertion SIO_000772 12517792 NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_assertion wasDerivedFrom befree-20140225 NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_assertion wasGeneratedBy ECO_0000203 NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP872822.RAh0rkk2jtGMM5K39vyEeUZBLxWy0pIRvVrjlEAOlPAhE130_provenance.