@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms> .
@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:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_head {
  this: np:hasAssertion dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion;
    np:hasProvenance dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance;
    np:hasPublicationInfo dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion a np:Assertion .
  
  dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance a np:Provenance .
  
  dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1332347 a ncit:C7057 .
  
  dgn-gda:DGN0329aeaf42b7572dd6c7042e1a69c9af sio:SIO_000628 miriam-gene:672, lld:C1332347;
    a sio:SIO_001121 .
}

dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance {
  dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion dcterms:description
      "[In this review, progress in the understanding of lobular carcinoma in situ and atypical ductal hyperplasia, the use of the molecular marker CerbB2, and information gained from the morphological analysis of tumours arising in patients with BRCA1 and BRCA2 mutations is discussed.]. 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:11577167;
    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:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:17+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" .
}