@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg> .
@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:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_head {
  this: np:hasAssertion dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_assertion;
    np:hasProvenance dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_provenance;
    np:hasPublicationInfo dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_assertion a np:Assertion .
  
  dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_provenance a np:Provenance .
  
  dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_assertion {
  miriam-gene:3304 a ncit:C16612 .
  
  lld:C0010346 a ncit:C7057 .
  
  dgn-gda:DGN4bf9a2b077503d7a0318b2d3e8fd814e sio:SIO_000628 miriam-gene:3304, lld:C0010346;
    a sio:SIO_001122 .
}

dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_provenance {
  dgn-np:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_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:NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}