Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion> ?p ?o ?g. }
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- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion type Assertion NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_head.
- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_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." NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_provenance.
- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion evidence source_evidence_literature NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_provenance.
- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion SIO_000772 10586249 NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_provenance.
- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion wasDerivedFrom befree-2016 NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_provenance.
- NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_assertion wasGeneratedBy ECO_0000203 NP269202.RAIfdb7Kb8tDX0j36-GUOPwRLvk0_P-0w7QAJtMfThEC0130_provenance.