Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_assertion description "[PINK1 was absent in cortical Lewy bodies, in neurofibrillary tangles in Alzheimer's disease, progressive supranuclear palsy and corticobasal degeneration, and in the glial and neuronal alpha-synuclein positive inclusions in multiple system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_assertion evidence source_evidence_literature NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_assertion SIO_000772 16702191 NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_assertion wasDerivedFrom befree-2016 NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_assertion wasGeneratedBy ECO_0000203 NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.
- befree-2016 importedOn "2016-02-19" NP549813.RA1cAGIu5wogVwHkkK1viIEw4Es45FcNfdnvuJ_tyve9s130_provenance.