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- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion type Assertion NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_head.
- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion description "[Recessive mutations in GJC2, the gene for Cx47, are one cause of Pelizaeus-Merzbacher-like disease (PMLD), which is characterized by nystagmus within the first 6 months of life, cerebellar ataxia by 4 years, and spasticity by 6 years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_provenance.
- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion evidence source_evidence_literature NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_provenance.
- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion SIO_000772 21871435 NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_provenance.
- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion wasDerivedFrom befree-2016 NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_provenance.
- NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_assertion wasGeneratedBy ECO_0000203 NP919545.RAeSHoMsUVWbhFa-8sTy9LhjXRbRTjVEin-tDKw6h2z4M130_provenance.