Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion type Assertion NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_head.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion wasGeneratedBy ECO_0000203 NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_provenance.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion wasDerivedFrom befree-20150227 NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_provenance.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion SIO_000772 24519899 NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_provenance.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion evidence source_evidence_literature NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_provenance.
- NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_assertion description "[Likewise, cases carrying a combination of variant genotypes of CYPs and GSM1 (null) were at higher risk (up to 5-fold) of developing HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436742.RAEdQGHnbjzD0iJHYbgACLMvYf52dSMLOkun3BEilSsjo130_provenance.