Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion> ?p ?o ?g. }
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- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion type Assertion NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_head.
- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_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." NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.
- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion evidence source_evidence_literature NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.
- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion SIO_000772 24878226 NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.
- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion wasDerivedFrom befree-2016 NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.
- NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion wasGeneratedBy ECO_0000203 NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.