Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_assertion description "[GAP-43 levels were low in all disorders analysed (in particular motor neuron disease; p=0.001, and movement disorders and multiple sclerosis; p<0.0001) compared to controls, aside from CNS infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_assertion evidence source_evidence_literature NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_assertion SIO_000772 25175067 NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_assertion wasDerivedFrom befree-20150227 NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_assertion wasGeneratedBy ECO_0000203 NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP417994.RAMXx5SzxW6gp_ECLQVBA1Oz91xGk0zbo8PsfxWKQRQqY130_provenance.