Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_assertion description "[These findings corroborate the clinical importance of the C9ORF72 mutation in frontotemporal lobar degeneration, delineate phenotypic and neuropathological features that could help to guide genetic testing, and suggest hypotheses for elucidating the neurobiology of a culprit subcortical network.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_assertion evidence source_evidence_literature NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_assertion SIO_000772 22366791 NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_assertion wasDerivedFrom befree-2016 NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_assertion wasGeneratedBy ECO_0000203 NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.
- befree-2016 importedOn "2016-02-19" NP963450.RAeVlsXvWb0XouZZ9GSx81G7sdsFII0a3Ga3OUvqOvEDA130_provenance.