Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP268330.RAN343ZqkGK8OCte0RlGWpVW_W0T7Aex6Nqjk8qBxM6tA#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 24519899 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[However, cases carrying haplotypes with variant alleles of both CYP1A1*2A and *2C or CYP1B1*2 and *3 or CYP2E1*5B and *6 were at significant risk of developing HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.