@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs> .
@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:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_head {
  this: np:hasAssertion dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_assertion;
    np:hasProvenance dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_provenance;
    np:hasPublicationInfo dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_assertion a np:Assertion .
  
  dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_provenance a np:Provenance .
  
  dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_assertion {
  miriam-gene:2261 a ncit:C16612 .
  
  lld:C0686619 a ncit:C7057 .
  
  dgn-gda:DGN898784db77bfae19ff21cef17d8d6995 sio:SIO_000628 miriam-gene:2261, lld:C0686619;
    a sio:SIO_001121 .
}

dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_provenance {
  dgn-np:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_assertion dcterms:description
      "[Macrodissection of individual tumours confirmed the presence of the FGFR3 mutant allele in non-invasive and invasive, low and high-grade regions of individual tumours and in the lymph node metastases of patients whose tumours possessed the characteristic morphological signature, suggesting that FGFR3 mutations are not restricted to the more clinically indolent regions of HGUCs.]. 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:21547910;
    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:NP705715.RA6zq_CvW5MuXGIMdf0MeiHfP6wvE7an9VdHdbXghmJAs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:09+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" .
}