@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc> .
@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:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_head {
  this: np:hasAssertion dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_assertion ;
    np:hasProvenance dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_provenance ;
    np:hasPublicationInfo dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_assertion a np:Assertion .
  dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_provenance a np:Provenance .
  dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  lld:C0178874 a ncit:C7057 .
  dgn-gda:DGNb199482260abc73129e375f1052da16e sio:SIO_000628 miriam-gene:2896 , lld:C0178874 ;
    a sio:SIO_001121 .
}
dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_provenance {
  dgn-np:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_assertion dcterms:description "[Given the similarities between the molecular mechanisms underlying cell status changes in tumorigenesis and development, application of GRN paradigms to tumor progression is particularly apt and offers the hope of providing a more concise, reliable, and therapeutically useful series of predictions linking gene regulation and tumor progression.]. 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:18952290 ;
    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:NP767248.RAPQpMhFVEg-PsLs5kyIYPQNxE_BIZKS2tQJom8BrwUDc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}