@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ> .
@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:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_head {
  this: np:hasAssertion dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion;
    np:hasProvenance dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance;
    np:hasPublicationInfo dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion a np:Assertion .
  
  dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance a np:Provenance .
  
  dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion {
  miriam-gene:30811 a ncit:C16612 .
  
  lld:C0018939 a ncit:C7057 .
  
  dgn-gda:DGN45f03fb52a4b418ca2de6ae9c1d9f33c sio:SIO_000628 miriam-gene:30811, lld:C0018939;
    a sio:SIO_001121 .
}

dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_provenance {
  dgn-np:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_assertion dcterms:description
      "[We conclude that patients with hematological disease have higher seropositive rates for B19 than occur in normal controls and that study of occult parvovirus B19 infection is recommended in patients with hematological disease.]. 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:14556276;
    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:NP705288.RAQavTRqHRb7UKciF2LjIbxNHIx3VoMNVxk9S1PHDFBSQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}