Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_assertion description "[A novel putative PGRN mutation leading to an amino acidic substitution was identified in a patient with clinical AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_assertion evidence source_evidence_literature NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_assertion SIO_000772 18752597 NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_assertion wasDerivedFrom gad-20150221 NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_assertion wasGeneratedBy ECO_0000203 NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129158.RA_VBkGcGBXQWkRa0c9WM_IGUu-9DC2D1aRnLl_AzmxyA130_provenance.