Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_assertion description "[Array comparative genomic hybridization (CGH) demonstrated a 1.5-Mb terminal deletion of the long arm of chromosome 20, which included deletion of the KCNQ2 and CHRNA4 genes, both of which have been associated with specific epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_assertion evidence source_evidence_literature NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_assertion SIO_000772 23166088 NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_assertion wasDerivedFrom befree-20140225 NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_assertion wasGeneratedBy ECO_0000203 NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.
- befree-20140225 importedOn "2014-02-25" NP603675.RA8hKMLNA8Ow8aUemjgy0duHmSJ11O21b-2Zn-8ENeD58130_provenance.