@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0> .
@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:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_head {
  this: np:hasAssertion dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_assertion ;
    np:hasProvenance dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_provenance ;
    np:hasPublicationInfo dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_assertion a np:Assertion .
  dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_provenance a np:Provenance .
  dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_assertion {
  miriam-gene:118429 a ncit:C16612 .
  lld:C0206186 a ncit:C7057 .
  dgn-gda:DGN287116ccfe754cc00a4e2ee4d6d8c3db sio:SIO_000628 miriam-gene:118429 , lld:C0206186 ;
    a sio:SIO_001121 .
}
dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_provenance {
  dgn-np:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_assertion dcterms:description "[The method makes use of advances in molecular technology, including the use of synthetic oligonucleotides with digoxigenin labelling in an in situ hybridisation (ISH) reaction, which can be completed in 24 h. Using this method, sections from 15 of 17 patients clinically diagnosed as having OHL contained readily detectable EBV-DNA in small foci along the upper layers of the stratum spinosum.]. 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:1716319 ;
    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:NP232855.RANIgNgTaKhp8yRWM1zBJMaM07j6LYxkNTFMTCRLkpEk0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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> ;
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}