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- source_evidence_literature type ECO_0000212 NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP696946.RAsp8jdWQ0XNeH8RYWeSFOYfP7sh4tWfR9TKhEOdBa0ms130_provenance.