Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_assertion description "[We describe 2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_assertion evidence source_evidence_literature NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_assertion SIO_000772 17049295 NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_assertion wasDerivedFrom befree-2016 NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_assertion wasGeneratedBy ECO_0000203 NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.
- befree-2016 importedOn "2016-02-19" NP575021.RAq5Eg8qekAEHMVQFSxDAiO_UcW6RRUDFt-zkPS1yFd7o130_provenance.