@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU> .
@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:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_head {
  this: np:hasAssertion dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_assertion;
    np:hasProvenance dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_provenance;
    np:hasPublicationInfo dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_assertion a np:Assertion .
  
  dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_provenance a np:Provenance .
  
  dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_assertion {
  miriam-gene:3418 a ncit:C16612 .
  
  lld:C0038463 a ncit:C7057 .
  
  dgn-gda:DGNeffe4146061314fe6cd9d42fbcf45757 sio:SIO_000628 miriam-gene:3418, lld:C0038463;
    a sio:SIO_001121 .
}

dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_provenance {
  dgn-np:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_assertion dcterms:description
      "[Nevertheless, the significantly higher proviral load in patients with strongyloidiasis or IDH was due to an increase in the mean clone abundance, not to an increase in the number of infected clones.]. 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:23592987;
    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:NP225804.RAnOoAMMXc2HLo_p8iJHcWFy8bSu_U6TCGTDKUP1kGHPU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}