@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_head {
   this: np:hasAssertion dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_assertion ;
    np:hasProvenance dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_provenance ;
    np:hasPublicationInfo dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_publicationInfo ;
    a np:Nanopublication .
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}
dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_assertion {
   miriam-gene:4255 a ncit:C16612 .
  lld:C0152018 a ncit:C7057 .
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dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_provenance {
   dgn-np:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_assertion dcterms:description "[We compared the frequencies of polymorphisms in ten genes that have been hypothesized to have a role in risk of EC (CYP1A1, CYP2A6, CYP2E1, GSTM1, GSTP1, GSTT1, ADH2, ADH3, ALDH2, and O6-MGMT) among three Iranian ethnic groups with highly varying rates of EC.]. 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:15327835 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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  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:NP555440.RAWfG-lHdNOptoQdJWu0AWqTFITipPzah7aj5i5jxJFGg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:08+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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