Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_assertion description "[Mutation screening of RAD51C in high-risk breast and ovarian cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_assertion evidence source_evidence_literature NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_assertion SIO_000772 22476429 NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_assertion wasDerivedFrom befree-20150227 NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_assertion wasGeneratedBy ECO_0000203 NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663852.RAKlVG_hwnwJFbVsHU85VPEw4Vs6JbhnQO2STl4sogbfI130_provenance.