@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_head {
  this: np:hasAssertion dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_assertion ;
    np:hasProvenance dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_provenance ;
    np:hasPublicationInfo dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_assertion {
  miriam-gene:26246 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGN63e37fa342f0bcbbeb03aa9cde79b308 sio:SIO_000628 miriam-gene:26246 , lld:C0011847 ;
    a sio:SIO_001121 .
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dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_provenance {
  dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_assertion dcterms:description "[For the tagSNPs rs1360590, rs3217992, and rs518394, we could validate the associations with AgP before and after adjustment for the covariates smoking, gender and diabetes, with SNP rs3217992 being the most significant (OR 1.48, 95% CI 1.19 to 1.85; p=0.0004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP532274.RAUaD-UUr4yAPCWEpGynbc2LI3D5z9iynSV_y5AVcm-gg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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