Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_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." NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_assertion evidence source_evidence_literature NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_assertion SIO_000772 22176150 NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_assertion wasDerivedFrom befree-20150227 NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_assertion wasGeneratedBy ECO_0000203 NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568324.RAb0WVIhaM-EzBYcYfymfXWIAPkyhOydbLtqmRIhKIx3U130_provenance.