@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY> .
@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:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_head {
  this: np:hasAssertion dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_assertion;
    np:hasProvenance dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_provenance;
    np:hasPublicationInfo dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_assertion a np:Assertion .
  
  dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_provenance a np:Provenance .
  
  dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_assertion {
  miriam-gene:2048 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN28b526877d88a41ffb61af24367c4628 sio:SIO_000628 miriam-gene:2048, lld:C0027651;
    a sio:SIO_001123 .
}

dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_provenance {
  dgn-np:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_assertion dcterms:description
      "[Deregulated EphB2 expression may play a role in several cancer types with loss of EphB2 expression serving as an indicator of the possible pathogenetic role of EphB2 signaling in the maintenance of tissue architecture of colon epithelium.]. 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:16166419;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP111507.RAHTT2qOZvFLyNCZ2i9l64xsJwBlCSfnSB-lgT-6Mt8oY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:57+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" .
}