Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion description "[These results strongly suggest that contrary to previous studies, there is no significant effect of AIB1 genetic variation on BC risk in BRCA1 mutation carriers and provide an indication that there is also no strong risk modification in BRCA2 carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion evidence source_evidence_literature NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion SIO_000772 15900600 NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion wasDerivedFrom gad-20130706 NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_assertion wasGeneratedBy ECO_0000203 NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.
- gad-20130706 importedOn "2013-07-06" NP53952.RAyxpLBetUrUCiPO34K6rjaT0QJNuRpz9o69BcRGrbB1A130_provenance.