@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54> .
@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:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_head {
  this: np:hasAssertion dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion;
    np:hasProvenance dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance;
    np:hasPublicationInfo dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion a np:Assertion .
  
  dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance a np:Provenance .
  
  dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion {
  miriam-gene:3586 a ncit:C16612 .
  
  lld:C0010346 a ncit:C7057 .
  
  dgn-gda:DGN5a13944dede48714d5d0f097813d737f sio:SIO_000628 miriam-gene:3586, lld:C0010346;
    a sio:SIO_001122 .
}

dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance {
  dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion dcterms:description
      "[ Allele A of the Hsp70-2 gene may be associated with a less severe form of CD, suggesting the clinical value of the genotype assessment. The genetic determination of the defense mechanisms in CD appears to be associated with the polymorphism of the Hsp70-2 gene rather than that of the CD14 or IL-10 genes.]. 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:16165702;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}