Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_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." NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_assertion evidence source_evidence_literature NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_assertion SIO_000772 18438698 NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_assertion wasDerivedFrom befree-20150227 NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_assertion wasGeneratedBy ECO_0000203 NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.