@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk> .
@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:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_head {
  this: np:hasAssertion dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_assertion;
    np:hasProvenance dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_provenance;
    np:hasPublicationInfo dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_assertion a np:Assertion .
  
  dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_provenance a np:Provenance .
  
  dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0035439 a ncit:C7057 .
  
  dgn-gda:DGNc80a5788fee926e194242802d0c890d7 sio:SIO_000628 miriam-gene:3133, lld:C0035439;
    a sio:SIO_001121 .
}

dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_provenance {
  dgn-np:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_assertion dcterms:description
      "[The aim of the present investigation was to determine whether the alleles of the MHC class III complement proteins BF, C2 and C4 (C4A and C4B) could be markers for RHD in the Brazilian population.]. 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:7777829;
    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:NP506952.RANYrAmLbFcxXPaXDvES9qElKGKcQj92iHtcoLdFTFUIk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:02+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" .
}