Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_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." NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_assertion evidence source_evidence_literature NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_assertion SIO_000772 20738937 NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_assertion wasDerivedFrom gad-20150221 NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_assertion wasGeneratedBy ECO_0000203 NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184509.RA4Sp9VFdcHCmNuPhr-Fxj0vE6v3Mws1D4Tzd_ofnGRtE130_provenance.