Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_assertion description "[In conclusion, LPL-Pvu II polymorphism cannot be used as independent genetic risk factor for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_assertion evidence source_evidence_literature NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_assertion SIO_000772 17473385 NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_assertion wasDerivedFrom befree-20140225 NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_assertion wasGeneratedBy ECO_0000203 NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP620848.RALeCDcGVK_Vpj90Q1QXrSZvFmYkEagtsp_2KtlfH5zzA130_provenance.