@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA> .
@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:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_head {
  this: np:hasAssertion dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion;
    np:hasProvenance dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance;
    np:hasPublicationInfo dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion a np:Assertion .
  
  dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance a np:Provenance .
  
  dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion {
  miriam-gene:3117 a ncit:C16612 .
  
  lld:C0850024 a ncit:C7057 .
  
  dgn-gda:DGN47a000e1f8d013a4de960e5b41e5c7b5 sio:SIO_000628 miriam-gene:3117, lld:C0850024;
    a sio:SIO_001121 .
}

dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance {
  dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion dcterms:description
      "[The characteristic celiac HLA (DQA1 0501 DQB1 0201 heterodimer) was identified in five relatives with positive challenge (including the patient with more severe mucosal atrophy) but was also present in eight relatives with no evidence of gluten sensitivity in the rectal mucosa.]. 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:9260799;
    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:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}