@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4> .
@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/v4.0.0/void/> .

dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_head {
  this: np:hasAssertion dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_assertion;
    np:hasProvenance dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_provenance;
    np:hasPublicationInfo dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_assertion a np:Assertion .
  
  dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_provenance a np:Provenance .
  
  dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C1302401 a ncit:C7057 .
  
  dgn-gda:DGN889726cfc84d98565aea7462b8b8e58d sio:SIO_000628 miriam-gene:2944, lld:C1302401;
    a sio:SIO_001122 .
}

dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_provenance {
  dgn-np:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_assertion dcterms:description
      "[Although with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.]. 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:22161138;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP946029.RACeYdIb1us8FTxoy9Irdcs0cOP_MJD5PiR31x3kmTZM4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:53+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}