Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_assertion description "[For MMP9 R279Q (rs17576), modest pharmacogenetic findings were observed for combined CHD and the composite CVD outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_assertion evidence source_evidence_literature NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_assertion SIO_000772 21887284 NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_assertion wasDerivedFrom befree-20140225 NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_assertion wasGeneratedBy ECO_0000203 NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP660130.RAO9wAGULtRcUXfraQfZsgF6C793cY-dscty0s-ZQ5kdw130_provenance.