Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion> ?p ?o ?g. }
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- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion type Assertion NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_head.
- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion description "[This case illustrates the clinical heterogeneity that exists in neuropathies associated with MPZ mutations and highlights that in patients with mild hypotonia in the first months that develop a very severe demyelinating neuropathy, the MPZ gene must be taken into account.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion evidence source_evidence_literature NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion SIO_000772 22176150 NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion wasDerivedFrom befree-20140225 NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_assertion wasGeneratedBy ECO_0000203 NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.