Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion> ?p ?o ?g. }
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- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion type Assertion NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_head.
- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion wasGeneratedBy ECO_0000203 NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_provenance.
- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion wasDerivedFrom befree-20150227 NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_provenance.
- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion SIO_000772 24519899 NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_provenance.
- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_assertion evidence source_evidence_literature NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_provenance.
- NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_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." NP339779.RAhx3E4MKokTV3Fzeau-MQbc-ZcoIcoyKl6_D_co9RARI130_provenance.