Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.
- 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.
- ctd_human-20130708 importedOn "2013-07-24" NP9236.RAbm4jMrwOcef9tOgiUGWn4Na3XEljTO_SzHJ_-RMvlZE130_provenance.