@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8> .
@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:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_head {
  this: np:hasAssertion dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_assertion;
    np:hasProvenance dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_provenance;
    np:hasPublicationInfo dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_assertion a np:Assertion .
  
  dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_provenance a np:Provenance .
  
  dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  
  lld:C0038273 a ncit:C7057 .
  
  dgn-gda:DGN5bf4d0917a6c3b8c575f85d2355b0777 sio:SIO_000628 miriam-gene:3492, lld:C0038273;
    a sio:SIO_001121 .
}

dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_provenance {
  dgn-np:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_assertion dcterms:description
      "[To test the hypothesis that signaling through innate immunity receptors may influence the behavior of the malignant clone, we investigated the functional response triggered by the stimulation of TLRs and NOD2 in 67 CLL cases assigned to different subgroups on the basis of immunoglobulin heavy variable (IGHV ) gene usage, IGHV gene mutational status or B-cell receptor (BcR) stereotypy.]. 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:22437326;
    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:NP710112.RA_MQZD-FYNGm_HFai3BEoAOqn1I3rvhXFDXF-0MfZBl8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}