Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion> ?p ?o ?g. }
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- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion type Assertion NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_head.
- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion description "[In the field of the peripheral neuropathies we present data on a newly described autosomal recessive Charcot-Marie-Tooth disease (CMT4F) with mutations in the periaxin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_provenance.
- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion evidence source_evidence_literature NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_provenance.
- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion SIO_000772 12094560 NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_provenance.
- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion wasDerivedFrom befree-20150227 NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_provenance.
- NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_assertion wasGeneratedBy ECO_0000203 NP933038.RABBr4B4xORyYwF9cpXsEq7GI6A9z6E6Y_IfmI00MwEmQ130_provenance.