Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_assertion description "[Rare haplotypes at ATM (P(corr) = 0.044) and BARD1 (P(corr) = 0.012) were associated with ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_assertion evidence source_evidence_literature NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_assertion SIO_000772 19584272 NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_assertion wasDerivedFrom befree-2016 NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_assertion wasGeneratedBy ECO_0000203 NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.
- befree-2016 importedOn "2016-02-19" NP749882.RAFYPtaTwWwUa0UQRXTk4EUk3HUVCdLn1EDzP0Ad9sIwo130_provenance.