Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion> ?p ?o ?g. }
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- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion type Assertion NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_head.
- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion wasGeneratedBy ECO_0000203 NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_provenance.
- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion wasDerivedFrom befree-20140225 NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_provenance.
- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion SIO_000772 15110095 NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_provenance.
- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion evidence source_evidence_literature NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_provenance.
- NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_assertion description "[Although the found correlations are driven primarily by a small number of subjects possessing the homozygous variant constellation, the strong influence of this genotype indicates that the CYP1A2*1F polymorphism could play an important role in human cancer risk susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617014.RANLXmxdhHiSXWR-A2FjPMpTC232ZJm3CxjneET6Dtp8o130_provenance.