Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_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." NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_assertion evidence source_evidence_literature NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_assertion SIO_000772 21747397 NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_assertion wasDerivedFrom befree-20150227 NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_assertion wasGeneratedBy ECO_0000203 NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP797590.RAQUySm92JOHQhtQYPlTF4Kjv0HZUJiwMT6q5fdsVtFTo130_provenance.