@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI> .
@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:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_head {
  this: np:hasAssertion dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_assertion;
    np:hasProvenance dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_provenance;
    np:hasPublicationInfo dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_assertion a np:Assertion .
  
  dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_provenance a np:Provenance .
  
  dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_assertion {
  miriam-gene:2209 a ncit:C16612 .
  
  lld:C0037054 a ncit:C7057 .
  
  dgn-gda:DGN2001664a750203df82639d2b620e52dc sio:SIO_000628 miriam-gene:2209, lld:C0037054;
    a sio:SIO_001121 .
}

dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_provenance {
  dgn-np:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_assertion dcterms:description
      "[To extend our previous findings showing an imbalanced distribution of immunoglobulin G2 (IgG2) antibodies to Plasmodium falciparum merozoite surface protein 2 (MSP2) and a higher frequency of infection with multiple P. falciparum strains in Gabonese children with sickle cell trait (hemoglobin AS), human Fc gamma receptor (Fc gamma R) IIa (CD32) polymorphism and the rate of in vitro invasion of red blood cells (RBCs) from subjects with either hemoglobin AA or AS by multiple P. falciparum strains were investigated.]. 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:16267770;
    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:NP666501.RA_SWlTXqSggdEUH6GChXBA3i2pHSst8lCXS0eEPU0MQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:42+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" .
}