Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion> ?p ?o ?g. }
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- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion type Assertion NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_head.
- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion description "[The most common genetic cause of the inherited peripheral neuropathy Charcot-Marie-Tooth disease is the PMP22 duplication; otherwise, CNVs have been considered rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.
- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion evidence source_evidence_literature NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.
- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion SIO_000772 25648254 NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.
- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion wasDerivedFrom befree-2016 NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.
- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion wasGeneratedBy ECO_0000203 NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.