@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM> .
@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#> .
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  this: np:hasAssertion dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_assertion ;
    np:hasProvenance dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_provenance ;
    np:hasPublicationInfo dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  lld:C0271907 a ncit:C7057 .
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dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_provenance {
  dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_assertion dcterms:description "[We analyzed the impact of the polymorphisms in CYP4501A1 and GSTM1 and GSTT1 genes on the susceptibility and disease severity in 200 patients with AA and compared the frequency with the normal population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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 ;
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dgn-np:NP684155.RAHFw5nejv-BScau-1I51qFUSNbI4N99nEVGcuuRBCPnM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:56+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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