@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:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_head { this: np:hasAssertion dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_assertion; np:hasProvenance dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_provenance; np:hasPublicationInfo dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_publicationInfo; a np:Nanopublication . dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_assertion a np:Assertion . dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_provenance a np:Provenance . dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_publicationInfo a np:PublicationInfo . } dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_assertion { miriam-gene:84898 a ncit:C16612 . lld:C0011849 a ncit:C7057 . dgn-gda:DGNef4e2119680aa36b69d33ce5f8c803e4 sio:SIO_000628 miriam-gene:84898, lld:C0011849; a sio:SIO_001121 . } dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_provenance { dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_assertion dcterms:description "[Using statistical models, we selected a total of 12 SNPs with P-values <1 × 10(-6) that were associated with DR. After controlling for diabetes duration and hemoglobin A(1C), 9 of the 12 SNPs located on 5 chromosomal regions were found to be associated with DR. Five loci not previously associated with DR susceptibility were identified in and around the following genes: MYSM1 (Myb-like, SWIRM, and MPN domains 1) located on chromosome 1p (odds ratio [OR], 1.50; 95% confidence interval [CI], 1.03-2.20); PLXDC2 (plexin domain-containing 2) located on the chromosome 10p (OR, 1.67; 95% CI, 1.06-2.65); ARHGAP22 (Rho GTPase-activating protein 22) located on chromosome 10q (OR, 1.65; 95% CI, 1.05-2.60); and HS6ST3 (heparan sulfate 6-O-sulfotransferase 3) located on chromosome 13q (OR, 2.33; 95% CI, 1.13-4.77).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:21310492; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP668250.RAfDtpZjMpJcDhLukeOy4AFXRoE7pzGlG_mnweiKGzdno130_publicationInfo { this: dcterms:created "2014-10-02T12:38:43+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" . }