Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_assertion description "[ Carriers of the rare allele CRYAB-650*C had an increased likelihood of a noninflammatory, neurodegenerative phenotype characterized by a relatively rapid, primary progressive clinical disease course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_assertion evidence source_evidence_literature NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_assertion SIO_000772 14610128 NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_assertion wasDerivedFrom gad-20130706 NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_assertion wasGeneratedBy ECO_0000203 NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP46567.RAiC5Tt8iXFc9fclFnghatl5bWcwaw-38CqOlOJ1r1IAc130_provenance.