dgn-np:NP17524.RAbeAmxz2R5SM7s6UnfYHLK7jXnkjVZ0VY9PYSZHlog50130_provenance {
  dgn-np:NP17524.RAbeAmxz2R5SM7s6UnfYHLK7jXnkjVZ0VY9PYSZHlog50130_assertion dcterms:description "[In the combined analysis, risk of TGCT was significantly associated with markers at four previously unreported loci: 4q22.2 in HPGDS (per-allele odds ratio (OR) = 1.19, 95% confidence interval (CI) = 1.12-1.26; P = 1.11 A 10(-8)), 7p22.3 in MAD1L1 (OR = 1.21, 95% CI = 1.14-1.29; P = 5.59 A 10(-9)), 16q22.3 in RFWD3 (OR = 1.26, 95% CI = 1.18-1.34; P = 5.15 A 10(-12)) and 17q22 (rs9905704: OR = 1.27, 95% CI = 1.18-1.33; P = 4.32 A 10(-13) and rs7221274: OR = 1.20, 95% CI = 1.12-1.28; P = 4.04 A 10(-9)), a locus that includes TEX14, RAD51C and PPM1E.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_curated ;
    sio:SIO_000772 miriam-pubmed:23666239 ;
    prov:wasDerivedFrom dgn-void:ctd_human-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:ctd_human-20150221 pav:importedOn "2015-02-21"^^xsd:date .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}