@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_head { this: np:hasAssertion dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_assertion; np:hasProvenance dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_provenance; np:hasPublicationInfo dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_publicationInfo; a np:Nanopublication . dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_assertion a np:Assertion . dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_provenance a np:Provenance . dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_publicationInfo a np:PublicationInfo . } dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_assertion { miriam-gene:2944 a ncit:C16612 . lld:C0023418 a ncit:C7057 . dgn-gda:DGNa35610d68bbc9f38977a98ce159962dd sio:SIO_000628 miriam-gene:2944, lld:C0023418; a sio:SIO_001121 . } dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_provenance { dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_assertion dcterms:description "[Assuming a very low prior probability of 0.000001, similar to a probability assumed for a randomly selected single-nucleotide polymorphism in a genome-wide association study, and statistical power to detect an OR of 1.5, 4 associations were considered noteworthy as denoted by an FPRP value <0.2: GSTM1 null and bladder cancer (OR, 1.5; 95% CI, 1.3-1.6; P = 1.9 x 10(-14)), NAT2 slow acetylator and bladder cancer (OR, 1.46; 95% CI, 1.26-1.68; P = 2.5 x 10(-7)), MTHFR C677T and gastric cancer (OR, 1.52; 95% CI, 1.31-1.77; P = 4.9 x 10(-8)), and GSTM1 null and acute leukemia (OR, 1.20; 95% CI, 1.14-1.25; P = 8.6 x 10(-15)).]. 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:18505952; prov:wasDerivedFrom dgn-void:ctd_human-20130708; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^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 . } dgn-np:NP17411.RAsldrO6Ccy1CgktzkNZL_-6mCufG_KkjEbSRISqx-Xxw130_publicationInfo { this: dcterms:created "2014-10-02T12:32:06+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }