Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_assertion evidence source_evidence_literature NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_assertion SIO_000772 20738937 NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_assertion wasDerivedFrom gad-20150221 NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_assertion wasGeneratedBy ECO_0000203 NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184511.RAztXfgUbcN5r0HzfvGxsG_Lr_rkqneOEXCNBHky8gzkk130_provenance.