Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP834968.RATGng6iINXu9we7u8U0qX1VJWZnzfqZ2a80oM9Qj-PuY#assertion> ?p ?o ?g. }
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- assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 24878226 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.