@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c> .
@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:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_head {
  this: np:hasAssertion dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_assertion;
    np:hasProvenance dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_provenance;
    np:hasPublicationInfo dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_assertion a np:Assertion .
  
  dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_provenance a np:Provenance .
  
  dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0002448 a ncit:C7057 .
  
  dgn-gda:DGN4a618b994939feec3a784e151fabbb53 sio:SIO_000628 miriam-gene:7157, lld:C0002448;
    a sio:SIO_001121 .
}

dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_provenance {
  dgn-np:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_assertion dcterms:description
      "[There were 12 ameloblastomas (two peripheral, eight solid, and two unicystic) and three ameloblastic carcinoma studied for loss of heterozygosity of tumor suppressor genes on chromosomes 1p, 3p, 9p,10q, and 17p (L-myc, hOGG1, p16, pten, and p53).]. 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:15133474;
    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:NP188076.RA2ZrxQmGgebRM4huMhyGrQu3_6EAxueq0HdAT9XMgR4c130_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" .
}