@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE> .
@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:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_head {
  this: np:hasAssertion dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion;
    np:hasProvenance dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance;
    np:hasPublicationInfo dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion a np:Assertion .
  
  dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance a np:Provenance .
  
  dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  
  lld:C0002448 a ncit:C7057 .
  
  dgn-gda:DGNad593c44b9adc79032c5afe9afc186dc sio:SIO_000628 miriam-gene:5727, lld:C0002448;
    a sio:SIO_001121 .
}

dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance {
  dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion dcterms:description
      "[Only five other cases of association between ameloblastoma and NBCCS have been reported so far, suggesting that PTCH1 missense mutation might take part in the pathogenesis of keratocystic odontogenic tumors (KCOTs) as well as ameloblastomas.]. 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:22559979;
    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:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:05+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" .
}