@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ> .
@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:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_head {
  this: np:hasAssertion dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion ;
    np:hasProvenance dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion a np:Assertion .
  dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance a np:Provenance .
  dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion {
  miriam-gene:923 a ncit:C16612 .
  lld:C0280100 a ncit:C7057 .
  dgn-gda:DGN2d7c9d95951f6e9522d93329bda2ac8b sio:SIO_000628 miriam-gene:923 , lld:C0280100 ;
    a sio:SIO_001121 .
}
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance {
  dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion dcterms:description "[Furthermore, FISH analysis using cosmid LLNL12-NCO1-144G3, which maps at the CHOP locus, revealed that the chromosome 12 breakpoints in all cell lines of the three benign solid tumors that were tested were located distal to the chromosome 12 translocation breakpoint with the CHOP gene in myxoid liposarcoma cells with t(12;16).]. 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:8020967 ;
    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:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:05+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" .
}