@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA> .
@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:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_head {
  this: np:hasAssertion dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_assertion;
    np:hasProvenance dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_provenance;
    np:hasPublicationInfo dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_assertion a np:Assertion .
  
  dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_provenance a np:Provenance .
  
  dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGNaed7eb8bca07bbf3157950aeeed16cd6 sio:SIO_000628 miriam-gene:7428, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_provenance {
  dgn-np:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_assertion dcterms:description
      "[Five microsatellite markers D3S192, D3S966, D3S647, D3S1228 and D3S659 were selected on chromosome 3p because of high frequency of alterations reported in head and neck squamous cell carcinoma and the involvement of von Hippel Lindau (VHL) at 3p25-26 and the fragile histidine triad (FHIT) at 3p14.2 genes proven in many tumour types.]. 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:21450513;
    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:NP773281.RAZsDDX0odZQGqaH1o06g-2X5SdKNsXbKfqKx600oIAlA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:47+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" .
}