Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion> ?p ?o ?g. }
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- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion type Assertion NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_head.
- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion description "[Overall, this study shows that the I92V LITAF sequence variant would be a good candidate for a biomarker in the case of the CMT1A/HNPP disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_provenance.
- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion evidence source_evidence_literature NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_provenance.
- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion SIO_000772 25342198 NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_provenance.
- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion wasDerivedFrom befree-2016 NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_provenance.
- NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_assertion wasGeneratedBy ECO_0000203 NP1232249.RACsAo7ta2u_I9vXPIFSjsBbRGGQb_O3pZKJzUviBUN3s130_provenance.