Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_assertion description "[Genetic variation in a region on chromosome 11 that contains the candidate genes AMBRA1, DGKZ, CHRM4 and MDK was significantly associated with SCZ in the combined sample (n=11?540; P=3.89 � 10(-9), odds ratio (OR)=1.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_assertion evidence source_evidence_literature NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_assertion SIO_000772 21747397 NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_assertion wasDerivedFrom befree-20140225 NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_assertion wasGeneratedBy ECO_0000203 NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615232.RA7nyKQoAszPm8Se9jtPWeDrQ14KbcL4BCwWndg0CGLKk130_provenance.