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- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion type Assertion NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_head.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion wasGeneratedBy ECO_0000203 NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion wasDerivedFrom befree-2016 NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion SIO_000772 8128981 NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion evidence source_evidence_literature NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.