@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA> .
@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:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_head {
  this: np:hasAssertion dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_assertion;
    np:hasProvenance dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_provenance;
    np:hasPublicationInfo dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_assertion a np:Assertion .
  
  dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_provenance a np:Provenance .
  
  dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_assertion {
  miriam-gene:8581 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGNc8e4775cad53266cd020f82788d7f9ba sio:SIO_000628 miriam-gene:8581, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_provenance {
  dgn-np:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_assertion dcterms:description
      "[At the RNA level HNSCC associated antigens like the E48 antigen, allow the detection of rare HNSCC cells in blood and bone marrow and, it is hoped, also in lymph nodes and lymph node aspirates.]. 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:10857164;
    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:NP706132.RAjMhtL-EAdbUYfxqLCpDN7CcdGJqwxrQWNRxaJI1A0xA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:09+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" .
}