Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion> ?p ?o ?g. }
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- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion type Assertion NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_head.
- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion description "[Detailed analysis of the different PMP22 mutants revealed, in addition to the obvious myelinopathy, distal axonopathy as a characteristic feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_provenance.
- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion evidence source_evidence_literature NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_provenance.
- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion SIO_000772 10586249 NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_provenance.
- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion wasDerivedFrom befree-20150227 NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_provenance.
- NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_assertion wasGeneratedBy ECO_0000203 NP662275.RApbCRSZwWbz8HDcj6xdzi16_U-apfAkPhxZdjUgNbLXI130_provenance.