Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_assertion description "[Several mutations have been identified in ARX gene, which is responsible for a wide spectrum of phenotypes, including syndromic as well as non syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_assertion evidence source_evidence_literature NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_assertion SIO_000772 16762829 NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_assertion wasDerivedFrom befree-2016 NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_assertion wasGeneratedBy ECO_0000203 NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.
- befree-2016 importedOn "2016-02-19" NP553798.RAV69NjRdDdeO_eyCEBdmcQaJD2M1WmGn4e9Efwtow7e4130_provenance.