Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_assertion wasGeneratedBy ECO_0000203 NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_assertion wasDerivedFrom befree-20140225 NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_assertion SIO_000772 22578324 NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_assertion evidence source_evidence_literature NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_assertion description "[Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurodevelopmental disorders with contrasting anxiety phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP180205.RASl2D-x6igxXjIAg_rt1BXcA843LnUpOAILBhsbmInhQ130_provenance.