@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM> .
@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:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_head {
  this: np:hasAssertion dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion ;
    np:hasProvenance dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance ;
    np:hasPublicationInfo dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion a np:Assertion .
  dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance a np:Provenance .
  dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  lld:C1333190 a ncit:C7057 .
  dgn-gda:DGNd54a27261b6b7eb866ad9e1e054bb1a3 sio:SIO_000628 miriam-gene:5727 , lld:C1333190 ;
    a sio:SIO_001121 .
}
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance {
  dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion dcterms:description "[Recent advances in genetic and molecular research, i.e., PTCH1 mutations and involvement of the Hedgehog signaling pathway, have led to increased knowledge of OKC pathogenesis which hints at potential new treatment options, although the question of whether the OKC is a cyst or a cystic neoplasm is yet to be answered with certainty.]. 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:21270459 ;
    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:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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" .
}