Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_assertion description "[The overall results suggest that there may be a small excess risk of HCC in individuals with GSTT1 null and possibly also with GSTM1 null genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_assertion evidence source_evidence_literature NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_assertion SIO_000772 18065725 NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_assertion wasDerivedFrom befree-20150227 NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_assertion wasGeneratedBy ECO_0000203 NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441079.RAftNsKG6CkNlqb8ZXMJNeab3CqXA1YMB5M-YI0TX3LiM130_provenance.