Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion wasGeneratedBy ECO_0000203 NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion wasDerivedFrom befree-20150227 NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion SIO_000772 18499664 NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion evidence source_evidence_literature NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.
- NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975045.RA68NSBZHnNzFV5qX1JF1lKkhbM40ScYIFfu7hUm6ZiXo130_provenance.