@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg> .
@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:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_head {
  this: np:hasAssertion dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_assertion;
    np:hasProvenance dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_provenance;
    np:hasPublicationInfo dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_assertion a np:Assertion .
  
  dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_provenance a np:Provenance .
  
  dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_assertion {
  miriam-gene:3162 a ncit:C16612 .
  
  lld:C0024535 a ncit:C7057 .
  
  dgn-gda:DGNa651a64937d2c965bab35c2f7f9432d6 sio:SIO_000628 miriam-gene:3162, lld:C0024535;
    a sio:SIO_001121 .
}

dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_provenance {
  dgn-np:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_assertion dcterms:description
      "[These results represent the first report on CM genetic risk factors in Angolan children and suggest the novel hypothesis that genetic variants of the TGFB2 and HMOX1 genes may contribute to confer a specific risk of developing the CM syndrome in patients with severe P. falciparum malaria.]. 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:20585394;
    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:NP888715.RAvkZ1_Gss9MtI09KfSzZMR-CC7kfu0eLmgvaH6nKhLCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}