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- source_evidence_literature type ECO_0000212 NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_assertion description "[LS patients with MSH2 mutations are at an increased risk for not only UTUC but also BCa and could be offered appropriate screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_assertion evidence source_evidence_literature NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_assertion SIO_000772 22883484 NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_assertion wasDerivedFrom befree-20150227 NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_assertion wasGeneratedBy ECO_0000203 NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP570218.RAiCLGGTyLnysscbo7UkIvhcrGnudal0aC3rvD7U0JPIo130_provenance.