@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI> .
@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:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_head {
  this: np:hasAssertion dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_assertion;
    np:hasProvenance dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_provenance;
    np:hasPublicationInfo dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_assertion a np:Assertion .
  
  dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_provenance a np:Provenance .
  
  dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_assertion {
  miriam-gene:4015 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGN8a5e03fc1a43fc55a383c69c2a8de68b sio:SIO_000628 miriam-gene:4015, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_provenance {
  dgn-np:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_assertion dcterms:description
      "[The chromosomal locus of LOX, 5q23, is affected by loss of heterozygosity (LOH) in colon cancer, suggesting that the LOX gene could be affected by LOH and consequently, loss or reduction of LOX function contribute to the tumorigenic process.]. 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:11807790;
    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:NP388406.RAbhh5kR9L3qA1ln97VGeZWhXzdrP3nuVpSUN0B2APWhI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}