@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc> .
@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:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_head {
  this: np:hasAssertion dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_assertion;
    np:hasProvenance dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_provenance;
    np:hasPublicationInfo dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_assertion a np:Assertion .
  
  dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_provenance a np:Provenance .
  
  dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_assertion {
  miriam-gene:2735 a ncit:C16612 .
  
  lld:C0025149 a ncit:C7057 .
  
  dgn-gda:DGN21be00a6dcddc77f5622a7c80bb47b01 sio:SIO_000628 miriam-gene:2735, lld:C0025149;
    a sio:SIO_001121 .
}

dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_provenance {
  dgn-np:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_assertion dcterms:description
      "[Constitutive activation of hedgehog signaling, often caused by PTCH1 inactivation and leading to inappropriate activation of GLI target genes, is crucial for the development of several human tumors including basal cell carcinoma of the skin and medulloblastoma.]. 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:15521068;
    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:NP731602.RAROgpsFzVFgsr57TuPBnWvrs8e-4vI5aUt7s1VRimSfc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+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" .
}