Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_assertion description "[Evidence that a mutation in the MLH1 3'-untranslated region confers a mutator phenotype and mismatch repair deficiency in patients with relapsed leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_assertion evidence source_evidence_literature NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_assertion SIO_000772 18056700 NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_assertion wasDerivedFrom befree-2016 NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_assertion wasGeneratedBy ECO_0000203 NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.
- befree-2016 importedOn "2016-02-19" NP643325.RA7bAvuowbPuRXAvMdkprZJZ3PEtCPFfwnd2kk2QmeBqg130_provenance.