@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo> .
@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:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_head {
  this: np:hasAssertion dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion;
    np:hasProvenance dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance;
    np:hasPublicationInfo dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion a np:Assertion .
  
  dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance a np:Provenance .
  
  dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion {
  miriam-gene:619501 a ncit:C16612 .
  
  lld:C0260037 a ncit:C7057 .
  
  dgn-gda:DGN30515e56c9917d0f0db3749c1fb5b7dc sio:SIO_000628 miriam-gene:619501, lld:C0260037;
    a sio:SIO_001121 .
}

dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_provenance {
  dgn-np:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_assertion dcterms:description
      "[In order to clarify the origin of multiple tumors of HCC genetically, we examined patterns of loss of heterozygosity (LOH) on chromosome 16 for DNA isolated from 43 HCCs resected from 19 patients by analysis of restriction fragment length polymorphism.]. 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:1347253;
    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:NP855507.RApvRRsad-jMuHTKOXGHpqOjPqGxERIJtd3icxk-crcVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}