@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o> .
@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:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_head {
  this: np:hasAssertion dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_assertion;
    np:hasProvenance dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_provenance;
    np:hasPublicationInfo dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_assertion a np:Assertion .
  
  dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_provenance a np:Provenance .
  
  dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C0002382 a ncit:C7057 .
  
  dgn-gda:DGN098979beeccb7ca2c85d945a2fa028ed sio:SIO_000628 miriam-gene:3553, lld:C0002382;
    a sio:SIO_001121 .
}

dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_provenance {
  dgn-np:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_assertion dcterms:description
      "[These results suggest a molecular phenotype in which discrete sets of differentially expressed genes are associated with genetically determined susceptibility (Il1b, Tnf, and Stat6) or resistance (Il15 and Selp) to alveolar bone loss, providing insight into the genetic etiology of this complex 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:15271905;
    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:NP159651.RAZKMtiNRDFOTFGmZReyo2-14ntHK-_GTKfTB5QrM6N7o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:26+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" .
}