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- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion type Assertion NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_head.
- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion wasGeneratedBy ECO_0000203 NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_provenance.
- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion wasDerivedFrom befree-20150227 NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_provenance.
- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion SIO_000772 24727570 NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_provenance.
- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion evidence source_evidence_literature NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_provenance.
- NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_assertion description "[We report on the extensive phenotypic characterization of five Italian patients from four unrelated families carrying dominant heterozygous DNMT1 mutations linked to two distinct autosomal dominant diseases: hereditary sensory and autonomic neuropathy with dementia and hearing loss type IE (HSAN IE) and autosomal dominant cerebellar ataxia, deafness and narcolepsy (ADCA-DN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357484.RA-jBPnFEtY6EQ7OLLHuApy22PrOXXVWvx_QwHR8sRCVk130_provenance.