@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU> .
@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:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_head {
  this: np:hasAssertion dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion;
    np:hasProvenance dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance;
    np:hasPublicationInfo dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion a np:Assertion .
  
  dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance a np:Provenance .
  
  dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion {
  miriam-gene:6581 a ncit:C16612 .
  
  lld:C0027627 a ncit:C7057 .
  
  dgn-gda:DGNafc1cdf583f036da67313befbc562f5c sio:SIO_000628 miriam-gene:6581, lld:C0027627;
    a sio:SIO_001121 .
}

dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_provenance {
  dgn-np:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_assertion dcterms:description
      "[Collectively, our data reveal that SP cells in the CNE-2 cell line not only possess the properties of cancer stem cells, but also have more mesenchymal cell characteristics which are associated with epithelial mesenchymal transition (EMT) and cancer cell invasion and metastasis.]. 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:22552840;
    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:NP165711.RAWLlHPQfbGG-mfoQK0VvqGFgP2bP3BLYMP8DLPzYbxpU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}