@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs> .
@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:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_head {
  this: np:hasAssertion dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_assertion ;
    np:hasProvenance dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_provenance ;
    np:hasPublicationInfo dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_assertion a np:Assertion .
  dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_provenance a np:Provenance .
  dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_assertion {
  miriam-gene:4267 a ncit:C16612 .
  lld:C0272138 a ncit:C7057 .
  dgn-gda:DGN4ea05843588caa542c720b18f20b9e58 sio:SIO_000628 miriam-gene:4267 , lld:C0272138 ;
    a sio:SIO_001121 .
}
dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_provenance {
  dgn-np:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_assertion dcterms:description "[All of the members of the peripheral primitive neuroectodermal tumor family (Ewing sarcomas, neuroectodermal tumors of bone, peripheral neuroepitheliomas, and Askin tumors) have similar morphologic and immunophenotypical features (ie, the proliferation of small and medium-sized round cells in a fibrous background showing strong and diffuse immunohistochemical positivity for CD99), and the common cytogenetic abnormality of a nonrandom translocation involving the EWS gene and one of several members of the erythroblastosis virus transforming sequence family of transcription factors.]. 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:20495444 ;
    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:NP438253.RAF-LPHknC49_01hn8JAtbtiC7qqrLMuHYzpYBToGLEKs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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" .
}