@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_head {
  this: np:hasAssertion dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_assertion ;
    np:hasProvenance dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_provenance ;
    np:hasPublicationInfo dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_assertion a np:Assertion .
  dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_provenance a np:Provenance .
  dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_assertion {
  miriam-gene:5156 a ncit:C16612 .
  lld:C1636667 a ncit:C7057 .
  dgn-gda:DGN5088751f96c449bc4f77b28d3b10f923 sio:SIO_000628 miriam-gene:5156 , lld:C1636667 ;
    a sio:SIO_001121 .
}
dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_provenance {
  dgn-np:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_assertion dcterms:description "[The fourth edition of the WHO classification provides a framework to incorporate those neoplasms in which a genetic abnormality is a major defining criterion of the disease, such as those associated with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1, as well as for those in which no specific genetic defect has yet been discovered and which remain clinically and pathologically defined.]. 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:22160042 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP945879.RAR0EOae58g_bDi1J4FvJ7b0ixaEwdSxbbhYl1FyHOwCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:53+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}