@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74> .
@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:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_head {
  this: np:hasAssertion dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_assertion;
    np:hasProvenance dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_provenance;
    np:hasPublicationInfo dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_assertion a np:Assertion .
  
  dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_provenance a np:Provenance .
  
  dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_assertion {
  miriam-gene:6422 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGNd582ebe5927c23f990631f70afb72551 sio:SIO_000628 miriam-gene:6422, lld:C0025286;
    a sio:SIO_001121 .
}

dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_provenance {
  dgn-np:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_assertion dcterms:description
      "[The signature was composed of genes involved in the cell cycle (TMEM30B, CKS2, and UCHL1) and other pathways previously described as being altered in meningiomas, that is, WNT (SFRP1 and SFRP4) and transforming growth factor-β pathways (LTBP2 and LMO4).]. 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:22964784;
    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:NP339091.RAhMEHRtrAjPIWTikrJ_M0qbkQpwyX-kLkxWD8r3qAz74130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}