@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc> .
@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:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_head {
  this: np:hasAssertion dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion;
    np:hasProvenance dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance;
    np:hasPublicationInfo dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion a np:Assertion .
  
  dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance a np:Provenance .
  
  dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0020981 a ncit:C7057 .
  
  dgn-gda:DGNcaf97e8b077cf93ea4c7743e6477edc9 sio:SIO_000628 miriam-gene:4843, lld:C0020981;
    a sio:SIO_001121 .
}

dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance {
  dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion dcterms:description
      "[The recent identification of follicular helper T (T(FH)) cell as the cell of origin of this neoplasm represents a major step in our understanding of the pathobiological characteristics of the disease and should, in the future, clarify the diagnostic criteria for AITL and help to delineate its spectrum, especially from PTCL, not otherwise specified (PTCL, NOS).]. 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:19961485;
    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:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}