Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion evidence source_evidence_literature NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion SIO_000772 18438698 NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion wasDerivedFrom befree-2016 NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion wasGeneratedBy ECO_0000203 NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.
- befree-2016 importedOn "2016-02-19" NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.