@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M> .
@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:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_head {
  this: np:hasAssertion dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_assertion;
    np:hasProvenance dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_provenance;
    np:hasPublicationInfo dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_assertion a np:Assertion .
  
  dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_provenance a np:Provenance .
  
  dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_assertion {
  miriam-gene:5664 a ncit:C16612 .
  
  lld:C0030409 a ncit:C7057 .
  
  dgn-gda:DGNedfc35a90a975f924410cba9d285f2aa sio:SIO_000628 miriam-gene:5664, lld:C0030409;
    a sio:SIO_001121 .
}

dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_provenance {
  dgn-np:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_assertion dcterms:description
      "[Paracoccidioidomycosis (PCM), the most important human systemic mycosis in Latin America, is known to be caused by at least four different phylogenetic lineages within the Paracoccidioides brasiliensis complex, including S1, PS2, PS3, and Pb01-like group.]. 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:22927496;
    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:NP652879.RArKF2jH7SIGTpzncdedvGOS0fe3CTIYK7EGbwga7VR3M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}