Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_assertion description "[The magnitudes of stroke risk observed for factor V Leiden, ACE, MTHFR and prothrombin, but not PAI-1, polymorphisms, are consistent with risks associated with equivalent changes in activated protein C resistance, ACE activity, homocysteine, prothrombin, and PAI-1 levels, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_assertion evidence source_evidence_literature NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_assertion SIO_000772 20161734 NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_assertion wasDerivedFrom gad-20150221 NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_assertion wasGeneratedBy ECO_0000203 NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP164631.RAcSFx2yhXf6tc1mjNFuni0ibDxEcwlBXA_wkZVIdWDQ4130_provenance.