Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_assertion description "[The strongest association was detected with rs1340513 in the JMJD2C gene at 9p24.1 (P=0.007; corrected P=0.011) that is the same SNP associated with infantile autism (P=0.0007) in the autism genome project consortium (2007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_assertion evidence source_evidence_literature NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_assertion SIO_000772 20410850 NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_assertion wasDerivedFrom gad-20150221 NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_assertion wasGeneratedBy ECO_0000203 NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP173361.RAnmbC2nqGXhaQaRlfqGDtr6P6dde1vFG7frHU5pF71kA130_provenance.