Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_assertion description "[X-linked lissencephaly with corpus callosum agenesis and ambiguous genitalia in genotypic males is associated with mutations of the ARX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_assertion evidence source_evidence_literature NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_assertion SIO_000772 15921228 NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_assertion wasDerivedFrom befree-2016 NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_assertion wasGeneratedBy ECO_0000203 NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.
- befree-2016 importedOn "2016-02-19" NP496781.RADGqOcGpUHdFcvAi4Bu1gUldaK0XgIzwU-LwgwNuYlfE130_provenance.