Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion evidence source_evidence_literature NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion SIO_000772 22738016 NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion wasDerivedFrom befree-20150227 NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_assertion wasGeneratedBy ECO_0000203 NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959064.RAJZVLc9Rev6EY415Q5d2nll2ZIE8dJmNvBaklgWY1aG8130_provenance.