@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM> .
@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:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_head {
  this: np:hasAssertion dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion ;
    np:hasProvenance dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance ;
    np:hasPublicationInfo dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion a np:Assertion .
  dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance a np:Provenance .
  dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion {
  miriam-gene:6899 a ncit:C16612 .
  lld:C0008487 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance {
  dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion dcterms:description "[The aim of this study was to attempt to identify the molecular genetic events that are responsible for the pathogenesis of chordomas with particular focus on the FGFR signalling pathway on the basis of the evidence in the ascidian and Xenopus models that the expression of brachyury requires the activation of this pathway.]. 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:19407855 ;
    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:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:55+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> ;
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    pav:version "v2.1.0.0" .
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}