Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_assertion description "[Alexander disease (AD), a rare neurodegenerative disorder of the central nervous system, is characterized by the accumulation of cytoplasmic protein aggregates (Rosenthal fibers) composed of glial fibrillary acidic protein (GFAP) and small heat-shock proteins within astrocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_assertion evidence source_evidence_literature NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_assertion SIO_000772 17894839 NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_assertion wasDerivedFrom befree-2016 NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_assertion wasGeneratedBy ECO_0000203 NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.
- befree-2016 importedOn "2016-02-19" NP631792.RA2vQVK9KI4gS9HETtZHGzK3VKWLDIyeOLN-_a7bT6Lw0130_provenance.