Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion> ?p ?o ?g. }
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- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion type Assertion NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_head.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion description "[Mohr-Tranebjaerg syndrome (MTS/DFN-1, deafness/dystonia syndrome) results from a mutation in deafness/dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a) and loss of the 70 kDa complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion evidence source_evidence_literature NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion SIO_000772 15254020 NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion wasDerivedFrom befree-2016 NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.
- NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_assertion wasGeneratedBy ECO_0000203 NP451958.RA2lrvfNrgSaJL7IAul7em6Jcnn0CwN40sUVQ-ttEeTQ0130_provenance.