Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_assertion description "[No mutation was detected and therefore mutations in HSD17B2 do not explain why some breast tumours exhibit low 17HSD type 2 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_assertion evidence source_evidence_literature NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_assertion SIO_000772 17260097 NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_assertion wasDerivedFrom befree-20140225 NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_assertion wasGeneratedBy ECO_0000203 NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586842.RAXQWYRrmLpmGSdWHQWXnCVY52REDPrt-02c226ahWy7A130_provenance.