Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_assertion description "[We conclude that molecular diagnosis is a necessary adjunct for clinical diagnosis and management of inherited and sporadic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_assertion evidence source_evidence_literature NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_assertion SIO_000772 11835375 NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_assertion wasDerivedFrom gad-20130706 NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_assertion wasGeneratedBy ECO_0000203 NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52648.RACMAe__FkGxKlYlBSl4qJLXgyqvk72fITZNnPnD1npwQ130_provenance.