Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_assertion description "[Our results indicate that polymorphism in the GSTM3 may be an important biomarker for PC risk, especially in the definition of the genetic risk profile of populations of southern Europe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_assertion evidence source_evidence_literature NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_assertion SIO_000772 14968442 NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_assertion wasDerivedFrom befree-20150227 NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_assertion wasGeneratedBy ECO_0000203 NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.
- befree-20150227 importedOn "2015-02-27" NP439055.RAbSL2nONwMMP3IN9KKSONELThsHhVYhS6xh3t6VXtNog130_provenance.