Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_assertion wasGeneratedBy ECO_0000203 NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_assertion wasDerivedFrom befree-20150227 NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_assertion SIO_000772 23160955 NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_assertion evidence source_evidence_literature NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.
- NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_assertion description "[Our data support associations between specific genes and reciprocal subphenotypes (CHD8-macrocephaly and DYRK1A-microcephaly) and replicate the importance of a β-catenin-chromatin-remodeling network to ASD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362722.RABWcAw9gakhYOqajc3L3bWBdxsvLX9mv5cLaIBt9e56U130_provenance.