@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ> .
@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:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_head {
  this: np:hasAssertion dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion;
    np:hasProvenance dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance;
    np:hasPublicationInfo dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion a np:Assertion .
  
  dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance a np:Provenance .
  
  dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion {
  miriam-gene:6469 a ncit:C16612 .
  
  lld:C0004779 a ncit:C7057 .
  
  dgn-gda:DGN8f0ca64cff2cd42d255fc0aa0d845ee9 sio:SIO_000628 miriam-gene:6469, lld:C0004779;
    a sio:SIO_001121 .
}

dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance {
  dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion dcterms:description
      "[Loss-of-function mutations in Patched (Ptch1) are implicated in constitutive activation of the Sonic hedgehog pathway in human basal cell carcinomas (BCCs), and inherited Ptch1 mutations underlie basal cell nevus syndrome in which a typical feature is multiple BCC occurring with greater incidence in portals of radiotherapy.]. 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:14871823;
    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:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}