Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_assertion description "[Families who carried the c.942+3A>T MSH2 gene mutation had a higher frequency of Muir-Torre syndrome than families who carried other mutations in the MSH2 gene (75% vs 25%; P = .026).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_assertion evidence source_evidence_literature NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_assertion SIO_000772 18270343 NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_assertion wasDerivedFrom befree-20140225 NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_assertion wasGeneratedBy ECO_0000203 NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676307.RAGeC2BHuqzSDCsBrtojjoDVPwNWTnjNN89xAimlgkH3U130_provenance.