@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y> .
@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:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_head {
  this: np:hasAssertion dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_assertion;
    np:hasProvenance dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_provenance;
    np:hasPublicationInfo dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_assertion a np:Assertion .
  
  dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_provenance a np:Provenance .
  
  dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_assertion {
  miriam-gene:5781 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNe10314adb992210db94c0e49638379c7 sio:SIO_000628 miriam-gene:5781, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_provenance {
  dgn-np:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_assertion dcterms:description
      "[In this cross-sectional study, we investigated patients in Sao Paulo, Brazil with leukaemia to determine the molecular frequency of B19 variants and characterize the viral genetic variability by partial and complete sequencing of the coding of non-structural protein 1 (NS1)/viral capsid proteins 1 and 2 (VP1/VP2).]. 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:23167493;
    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:NP173717.RAxo7z1XaBElbEvjpxcWsd1VCc9vPDb0WTZcytIEUbH-Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}