@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs> .
@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:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_head {
  this: np:hasAssertion dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_assertion;
    np:hasProvenance dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_provenance;
    np:hasPublicationInfo dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_assertion a np:Assertion .
  
  dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_provenance a np:Provenance .
  
  dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGNe78ab58a8fca0d3f670ee1929dde58ad sio:SIO_000628 miriam-gene:5925, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_provenance {
  dgn-np:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_assertion dcterms:description
      "[Analysis of clinical breast cancer samples showed that most of the cells contained two copies of the RB1 gene, even when restriction fragment length polymorphism analysis showed loss of heterozygosity (LOH) at the RB1 locus.]. 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:1354594;
    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:NP188731.RA5SXaJceJE1lAxm1bsxyxGYk-0RN5v_2R1Y71KYOL3cs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}