@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys> .
@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:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_head {
  this: np:hasAssertion dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_assertion;
    np:hasProvenance dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_provenance;
    np:hasPublicationInfo dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_assertion a np:Assertion .
  
  dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_provenance a np:Provenance .
  
  dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_assertion {
  miriam-gene:8718 a ncit:C16612 .
  
  lld:C1527336 a ncit:C7057 .
  
  dgn-gda:DGN917739d1682448e5bd435970a8b04e04 sio:SIO_000628 miriam-gene:8718, lld:C1527336;
    a sio:SIO_001121 .
}

dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_provenance {
  dgn-np:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_assertion dcterms:description
      "[The HLA and Gm haplotypes did not necessarily segregate persons into those with Sjögren's syndrome, other autoimmune disorders, or serologic abnormalities, but HLA alleles DR3 and DR2 occurred in significant excess in relatives with Sjögren's syndrome, irrespective of HLA haplotype.]. 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:6437309;
    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:NP334035.RAPRkVCaYBy8yZ6Gz7WRhgP0S9-jphttbjH4NJXq5o_ys130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:16+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" .
}