Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_assertion description "[There were no differences in the frequencies of the GSTM1 and GSTT1 null genotypes, and the slow acetylator genotype, between hypersensitive and non-sensitive patients, while GSTP1 frequency was lower (although non-significant) in the hypersensitive group [21% versus 32%, odds ratio (OR) = 0.5, Pc = 0.24].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_assertion evidence source_evidence_literature NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_assertion SIO_000772 11186133 NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_assertion wasDerivedFrom befree-20150227 NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_assertion wasGeneratedBy ECO_0000203 NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP438556.RAfi8XAwcjqQiIMuHXwu3MxVY0-u-Ods-KoD4rix6eeqU130_provenance.