@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM> .
@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:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_head {
  this: np:hasAssertion dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion ;
    np:hasProvenance dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance ;
    np:hasPublicationInfo dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion a np:Assertion .
  dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance a np:Provenance .
  dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion {
  miriam-gene:3577 a ncit:C16612 .
  lld:C0034186 a ncit:C7057 .
  dgn-gda:DGNb0ec6292e67851f5988ea57b31f9d1fc sio:SIO_000628 miriam-gene:3577 , lld:C0034186 ;
    a sio:SIO_001121 .
}
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance {
  dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion dcterms:description "[Here we discuss the mechanisms of neutrophil-mediated, chemokine receptor (CXCR1)-dependent clearance, and the defect in interleukin-8 receptor homolog knock-out (IL-8Rh KO) mice and describe the data linking low CXCR1 expression to recurrent pyelonephritis in man, as well as the information on the genetic basis for low CXCR1 expression in affected patients.]. 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:11817650 ;
    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:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}