@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I> .
@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:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_head {
  this: np:hasAssertion dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_assertion;
    np:hasProvenance dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_provenance;
    np:hasPublicationInfo dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_assertion a np:Assertion .
  
  dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_provenance a np:Provenance .
  
  dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_assertion {
  miriam-gene:846 a ncit:C16612 .
  
  lld:C0340164 a ncit:C7057 .
  
  dgn-gda:DGN403bec9cb33c173218b12d3a83513ccf sio:SIO_000628 miriam-gene:846, lld:C0340164;
    a sio:SIO_001121 .
}

dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_provenance {
  dgn-np:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_assertion dcterms:description
      "[Based on this finding, we investigated a possible association of the HHC haplotype and its marker alleles in an extended German sarcoidosis sample that comprised 995 German sarcoidosis families including individuals with the chronic and acute form of the disease, further refined to patients with and without Löfgren's syndrome.]. 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:18311470;
    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:NP357276.RALl1Tyg1z9VyJuinIZg_0KC5d5MpiHAbpliXK9qe6i4I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:29+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" .
}