@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ> .
@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:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_head {
  this: np:hasAssertion dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_assertion;
    np:hasProvenance dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_provenance;
    np:hasPublicationInfo dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_assertion a np:Assertion .
  
  dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_provenance a np:Provenance .
  
  dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C0483368 a ncit:C7057 .
  
  dgn-gda:DGN4e11166d8ff64a983604dcf30b0ee623 sio:SIO_000628 miriam-gene:1437, lld:C0483368;
    a sio:SIO_001121 .
}

dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_provenance {
  dgn-np:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_assertion dcterms:description
      "[The diagnosis was made by specific polymerase chain reaction amplification of aoHGE sequences from samples of the patient's blood and cerebrospinal fluid (CSF), as well as propagation of aoHGE in culture of HL60 cells inoculated with the patient's CSF.]. 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:11073767;
    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:NP371507.RAQ3J7xRuPSDJHZWDD3Di-2gwg5ThqmBDD_6JdXxhltKQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:37+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" .
}