Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_assertion description "[The difference of KIR genotypes between GD patients and healthy controls may explain the pathogenesis of GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_assertion evidence source_evidence_literature NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_assertion SIO_000772 19664392 NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_assertion wasDerivedFrom gad-20150221 NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_assertion wasGeneratedBy ECO_0000203 NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP96723.RAPScwi8LyB2TcTQ8gvZ7XVd1-UoXcAkVHh0tTs-OIDlk130_provenance.