Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion> ?p ?o ?g. }
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- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion type Assertion NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_head.
- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.
- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion evidence source_evidence_literature NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.
- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion SIO_000772 19293842 NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.
- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion wasDerivedFrom befree-20140225 NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.
- NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_assertion wasGeneratedBy ECO_0000203 NP168558.RADEO5yhM6TmvDNJbFfz5i8uZAMJdrLx-3glQYhbxOP7U130_provenance.