@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM> .
@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:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_head {
  this: np:hasAssertion dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_assertion;
    np:hasProvenance dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_provenance;
    np:hasPublicationInfo dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_assertion a np:Assertion .
  
  dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_provenance a np:Provenance .
  
  dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_assertion {
  miriam-gene:6608 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN879cda61aa5c17ece7da17b4207bffd6 sio:SIO_000628 miriam-gene:6608, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_provenance {
  dgn-np:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_assertion dcterms:description
      "[It now appears that constitutive activation of Hedgehog signalling, by inactivating mutations in PTCH1 or activating mutations in the coreceptor SMOH, is required and possibly sufficient for basal cell carcinoma development and also contributes to the formation of a variety of other tumour types, including medulloblastoma and rhabdomyosarcoma.]. 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:11130178;
    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:NP508549.RAHoZgbAHOV5veDNo-apDkCLorO4Q1spHbODmISdUfRiM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}