Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_assertion description "[An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_assertion evidence source_evidence_literature NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_assertion SIO_000772 22181065 NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_assertion wasDerivedFrom befree-2016 NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_assertion wasGeneratedBy ECO_0000203 NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.
- befree-2016 importedOn "2016-02-19" NP947840.RAes1z_sCds6PJGdQ2xtL5Bx9ABnLDX0A-nZ9hR0JKhII130_provenance.