Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion> ?p ?o ?g. }
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- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion type Assertion NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_head.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion description "[Charcot-Marie-Tooth type 1B (CMT1B) is a demyelinating neuropathy caused by mutations in the myelin protein zero (MPZ) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion evidence source_evidence_literature NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion SIO_000772 21940171 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion wasDerivedFrom befree-2016 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion wasGeneratedBy ECO_0000203 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.