@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q> .
@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:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_head {
  this: np:hasAssertion dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion;
    np:hasProvenance dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance;
    np:hasPublicationInfo dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion a np:Assertion .
  
  dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance a np:Provenance .
  
  dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion {
  miriam-gene:729230 a ncit:C16612 .
  
  lld:C0002895 a ncit:C7057 .
  
  dgn-gda:DGN27447c8275fe80d72f1ac58a7fa22772 sio:SIO_000628 miriam-gene:729230, lld:C0002895;
    a sio:SIO_001122 .
}

dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_provenance {
  dgn-np:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_assertion dcterms:description
      "[In order to contribute to the identification of the genetic differences underlying this phenotypic diversity in SCD, we proposed to study the distribution of polymorphic variants of the genes encoding the chemokine receptors CCR2 and CCR5, as well as three polymorphisms in the NOS3 gene, in Brazilian SCD 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:16305685;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63906.RAaGoUxjbJIVLDTGQPfMf6mcWamxcYRxHchHj_6NfTj2Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}