Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion type Assertion NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_head.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion description "[A haplotype near ASIP, known to affect a similar spectrum of pigmentation traits as MC1R variants, conferred significant risk of CM (odds ratio (OR) = 1.45, P = 1.2 x 10(-9)) and BCC (OR = 1.33, P = 1.2 x 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion evidence source_evidence_curated NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion SIO_000772 18488027 NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion wasDerivedFrom ctd_human-20130708 NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_assertion wasGeneratedBy ECO_0000218 NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.