Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion> ?p ?o ?g. }
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- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion type Assertion NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_head.
- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion wasGeneratedBy ECO_0000203 NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_provenance.
- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion wasDerivedFrom befree-20150227 NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_provenance.
- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion SIO_000772 24727570 NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_provenance.
- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_assertion evidence source_evidence_literature NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_provenance.
- NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_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." NP948506.RAAlzac5sG7xUElfpvWZUag-jGGoFRlbAD2chLrmUY80k130_provenance.