@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g> .
@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:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_head {
  this: np:hasAssertion dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_assertion;
    np:hasProvenance dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_provenance;
    np:hasPublicationInfo dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_assertion a np:Assertion .
  
  dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_provenance a np:Provenance .
  
  dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_assertion {
  miriam-gene:3577 a ncit:C16612 .
  
  lld:C0520575 a ncit:C7057 .
  
  dgn-gda:DGNb986e90d5cd7266e9ca647ec341be396 sio:SIO_000628 miriam-gene:3577, lld:C0520575;
    a sio:SIO_001121 .
}

dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_provenance {
  dgn-np:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_assertion dcterms:description
      "[For example, genetic alterations that reduce TLR4 function are associated with ABU, while polymorphisms reducing IRF3 or CXCR1 expression are associated with acute pyelonephritis and an increased risk for renal scarring.]. 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:22327887;
    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:NP900645.RAW0Qu2RlkNk3e1izhJ26tr-A1p_5biAva2Uk1RbXry0g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}