Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion> ?p ?o ?g. }
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- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion type Assertion NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_head.
- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion wasGeneratedBy ECO_0000203 NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_provenance.
- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion wasDerivedFrom befree-20150227 NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_provenance.
- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion SIO_000772 20976668 NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_provenance.
- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion evidence source_evidence_literature NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_provenance.
- NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_assertion description "[Hereditary neuropathy with liability to pressure palsies (HNPP), Charcot-Marie Tooth disease type 1A (CMT1A), Dejerine-Sottas syndrome, and congenital hypomyelinating neuropathy are all associated with defects in PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632455.RAASOgISpwOyvJzvPfVBGG3WYR_psekvvx9_nLm-Lf3WM130_provenance.