@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY> .
@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:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_head {
  this: np:hasAssertion dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion;
    np:hasProvenance dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance;
    np:hasPublicationInfo dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion a np:Assertion .
  
  dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance a np:Provenance .
  
  dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion {
  miriam-gene:3126 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGN649d29393a2678e8974a0771bb3c8d6c sio:SIO_000628 miriam-gene:3126, lld:C0007570;
    a sio:SIO_001121 .
}

dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance {
  dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion dcterms:description
      "[The need for an early and accurate diagnosis in celiac disease (CD) has focused attention on new diagnostic approaches, based on the efficiency of serological markers and the high negative predictive value of human leukocyte antigen (HLA) non-DQ2/8.]. 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:23111763;
    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:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}