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- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion type Assertion NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_head.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion description "[Phenotypic divergence is exemplified by different CLN8 mutations giving rise to two very different diseases, the mild CLN8 disease, EPMR (progressive epilepsy with mental retardation), and the more severe CLN8 disease, late infantile variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion evidence source_evidence_literature NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion SIO_000772 21990111 NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion wasDerivedFrom befree-20140225 NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.
- NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_assertion wasGeneratedBy ECO_0000203 NP617526.RAplWFctfKM6UbAIqKAAofLWntwNXzPqAjD0QUEqVphh0130_provenance.