@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k> .
@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:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_head {
  this: np:hasAssertion dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion;
    np:hasProvenance dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance;
    np:hasPublicationInfo dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion a np:Assertion .
  
  dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance a np:Provenance .
  
  dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion {
  miriam-gene:7294 a ncit:C16612 .
  
  lld:C1621958 a ncit:C7057 .
  
  dgn-gda:DGNb7af02e6ce1c3502215cbefdd63b2dd6 sio:SIO_000628 miriam-gene:7294, lld:C1621958;
    a sio:SIO_001121 .
}

dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance {
  dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion dcterms:description
      "[Because the heterotopic-to-orthotopic transfer and propagation of glioblastoma multiforme preserves the receptor tyrosine kinase (RTK) gene amplification of patient tumors, this approach should facilitate investigations for determining the extent to which RTK amplification status influences tumor response to RTK-directed therapies.]. 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:15831234;
    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:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}