Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_assertion wasGeneratedBy ECO_0000203 NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_assertion wasDerivedFrom lhgdn-20090331 NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_assertion SIO_000772 17650440 NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_assertion evidence source_evidence_literature NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_assertion description "[heterozygous carriers of FVL who experience an episode of venous thromboembolism (VTE) have on average a 40% increased risk of recurrent VTE over non-carriers; risk is lower with heterozygosity of prothrombin G20210A mutation [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP131286.RAL2U_cAW805cA4jMLj2b_Qq70VJWUhbq-1oaVNfpg26A130_provenance.