Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion> ?p ?o ?g. }
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- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion type Assertion NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_head.
- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion description "[We genotyped 146 Caucasian Lynch syndrome mutation carriers for a 5'-untranslated region polymorphism in cytochrome P450 17A1 (CYP17; c.-34T-->C) and an exon 4 polymorphism in catechol O-methyltransferase (COMT; c.472G-->A); 50 mutation carriers had developed colon or rectal cancer at last contact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_provenance.
- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion evidence source_evidence_literature NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_provenance.
- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion SIO_000772 17606708 NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_provenance.
- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion wasDerivedFrom befree-2016 NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_provenance.
- NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_assertion wasGeneratedBy ECO_0000203 NP618140.RAv0MoFcXNHCpO-dOYX-joP_O6VswJWZ9SsPiZZgf0EGc130_provenance.