@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg> .
@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:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_head {
  this: np:hasAssertion dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_assertion ;
    np:hasProvenance dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_provenance ;
    np:hasPublicationInfo dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_assertion a np:Assertion .
  dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_provenance a np:Provenance .
  dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_assertion {
  miriam-gene:118429 a ncit:C16612 .
  lld:C0038363 a ncit:C7057 .
  dgn-gda:DGNaa9b12d1565f0d9c678e0f354c8ea207 sio:SIO_000628 miriam-gene:118429 , lld:C0038363 ;
    a sio:SIO_001121 .
}
dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_provenance {
  dgn-np:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_assertion dcterms:description "[Therefore, the potential of HCMV as an etiologic agent in RAU was proposed and studies using the polymerase chain reaction (PCR) and in situ hybridization (ISH) have been performed to investigate the possible presence of HCMV DNA in pre-ulcerative oral aphthous lesions in patients with RAU or Behçet's disease (BD) of the mucocutaneous type.]. 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:8835817 ;
    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:NP708626.RAm2cmjo9CfZPCBjCUgT_hP4fdyaN8mFVBYrT_0ONT4xg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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" .
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}