Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_assertion description "[First, a Finnish study observed that the NAT2 slow acetylator phenotype was associated with an increased risk of MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_assertion evidence source_evidence_literature NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_assertion SIO_000772 18838334 NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_assertion wasDerivedFrom befree-20150227 NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_assertion wasGeneratedBy ECO_0000203 NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP944547.RAdXHuX-_WmL8a3QdgzLEsOLX8wtw4D4NoGsvAJ3FDZfY130_provenance.