@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU> .
@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:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_head {
  this: np:hasAssertion dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_assertion ;
    np:hasProvenance dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_provenance ;
    np:hasPublicationInfo dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_assertion a np:Assertion .
  dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_provenance a np:Provenance .
  dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_assertion {
  miriam-gene:729230 a ncit:C16612 .
  lld:C0001175 a ncit:C7057 .
  dgn-gda:DGN268e4990208758990f7e6abe192d6786 sio:SIO_000628 miriam-gene:729230 , lld:C0001175 ;
    a sio:SIO_001121 .
}
dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_provenance {
  dgn-np:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_assertion dcterms:description "[The objective of our study was to design a comprehensive mutation detection assay for the entire coding region of the CCR2A and CCR2B gene transcripts, including all relevant splice site junctions and to identify novel mutations and SNPs within our predominantly African-based population, which could influence an individual's susceptibility to HIV-1 infection and/or progression to AIDS.]. 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:12325020 ;
    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:NP397264.RATr3cq9UayrjV5VXze3kLy9EOxEMDFKGD_PeKD7KzwHU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:56+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" .
}