@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc> .
@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:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_head {
   this: np:hasAssertion dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_assertion ;
    np:hasProvenance dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_provenance ;
    np:hasPublicationInfo dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_assertion a np:Assertion .
  dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_provenance a np:Provenance .
  dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_assertion {
   miriam-gene:3125 a ncit:C16612 .
  lld:C0036202 a ncit:C7057 .
  dgn-gda:DGNf0a49cb41f674001547db7d6863eaa2e sio:SIO_000628 miriam-gene:3125 , lld:C0036202 ;
    a sio:SIO_001121 .
}
dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_provenance {
   dgn-np:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_assertion dcterms:description "[Frequency of HLA A2, A9, A24 (9), A25, A69 (28), B12, B22, B38, B49 (21), DR4, and DR14 antigens were significantly higher, and frequencies of HLA B7 and DR7 were significantly less in sarcoidosis patients.]. 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:17458393 ;
    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:NP375695.RAtJzbG1rXl5-MI-Ngj731Rl4coiPK51lnwGhKaBr7Vkc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:40+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" .
}