Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_assertion description "[Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_assertion evidence source_evidence_literature NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_assertion SIO_000772 17420019 NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_assertion wasDerivedFrom befree-20140225 NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_assertion wasGeneratedBy ECO_0000203 NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP429922.RAggD1FKLNYL-9sxwbofEqxGsP8Dg3umSdHjs7AMUFoHY130_provenance.