Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion> ?p ?o ?g. }
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- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion type Assertion NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_head.
- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_provenance.
- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion evidence source_evidence_literature NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_provenance.
- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion SIO_000772 10219749 NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_provenance.
- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion wasDerivedFrom befree-20140225 NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_provenance.
- NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_assertion wasGeneratedBy ECO_0000203 NP716292.RAhYcG6ySOfhX5agGW3NonNTqktIm0YByKpxb1Wpy4aCE130_provenance.