Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_assertion wasGeneratedBy ECO_0000203 NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_assertion wasDerivedFrom befree-2016 NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_assertion SIO_000772 24262325 NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_assertion evidence source_evidence_literature NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.
- NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_assertion description "[Because these loci had prior evidence for genome-wide significance for CAD, we specifically analyzed the respective signals for IS and LAS and found evidence for association at chr12q24/SH2B3 (PIS=1.62×10(-7)) and ABO (PIS=2.6×10(-4)), as well as at HDAC9 (PLAS=2.32×10(-12)), 9p21 (PLAS=3.70×10(-6)), RAI1-PEMT-RASD1 (PLAS=2.69×10(-5)), EDNRA (PLAS=7.29×10(-4)), and CYP17A1-CNNM2-NT5C2 (PLAS=4.9×10(-4)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130421.RAboXjvuru9qxSDOeQiA1oWEJG0POAkkjnDYZVBa0Wg4s130_provenance.