Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion wasGeneratedBy ECO_0000203 NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion wasDerivedFrom befree-2016 NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion SIO_000772 22739344 NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion evidence source_evidence_literature NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.
- NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_assertion description "[We expand the mutational spectrum in patients with FOXG1-related encephalopathies and precise the core FOXG1 syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993582.RAS-BrE1a_bL-FmlZSFpF1LbOMLpc7QBqUrwT2K7MdLZA130_provenance.