@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E> .
@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:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_head {
  this: np:hasAssertion dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion;
    np:hasProvenance dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance;
    np:hasPublicationInfo dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion a np:Assertion .
  
  dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance a np:Provenance .
  
  dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0010701 a ncit:C7057 .
  
  dgn-gda:DGN9c6e7548030a4cc3d24e9aba13a87055 sio:SIO_000628 miriam-gene:3342, lld:C0010701;
    a sio:SIO_001121 .
}

dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance {
  dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion dcterms:description
      "[We studied DNA copy number changes by CGH and allelic imbalance (AI) on 3p by LOH analysis on 22 phyllodes tumours (PT) of the breast in order to gain insight into the genetic basis of tumour progression in PT.]. 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:12632018;
    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:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}