@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q> .
@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:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_head {
  this: np:hasAssertion dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_assertion ;
    np:hasProvenance dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_assertion a np:Assertion .
  dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_provenance a np:Provenance .
  dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_assertion {
  miriam-gene:1233 a ncit:C16612 .
  lld:C0035435 a ncit:C7057 .
  dgn-gda:DGNd2d465e3728be4296254ca725bf2feea sio:SIO_000628 miriam-gene:1233 , lld:C0035435 ;
    a sio:SIO_001121 .
}
dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_provenance {
  dgn-np:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_assertion dcterms:description "[In this study, variation screening of the entire coding regions of CCR3 and CCR4 was performed, and possible association with several autoimmune diseases was tested, using the genomic DNA from 304 Japanese healthy individuals and 272 Japanese patients with rheumatic diseases.]. 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:11196669 ;
    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:NP308048.RAhqIvk2XR97LRKXg3V3elwtSMgUg6mgJw0Cswu6Dxt_Q130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:05+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" .
}