Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_assertion description "[ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_assertion evidence source_evidence_literature NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_assertion SIO_000772 23623388 NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_assertion wasDerivedFrom befree-2016 NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_assertion wasGeneratedBy ECO_0000203 NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1072806.RAkjt9sVQM8RcoBBbySMLE4wda0JHCfhPaTUVlsK3yahk130_provenance.