Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_assertion description "[We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_assertion evidence source_evidence_literature NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_assertion SIO_000772 21873549 NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_assertion wasDerivedFrom gad-20130706 NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_assertion wasGeneratedBy ECO_0000203 NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP85018.RAc_y_qeyz_GcrSdR_d7XlCDR--rJegtfJJg731HETZIQ130_provenance.