Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_assertion description "[Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_assertion evidence source_evidence_literature NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_assertion SIO_000772 16080119 NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_assertion wasDerivedFrom befree-2016 NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_assertion wasGeneratedBy ECO_0000203 NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.
- befree-2016 importedOn "2016-02-19" NP507364.RABh7Tf7nTFOvYV5DgouxRh9K8WCcWjVXI46CyKajIV-8130_provenance.