@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc> .
@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:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_head {
  this: np:hasAssertion dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_assertion;
    np:hasProvenance dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_provenance;
    np:hasPublicationInfo dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_assertion a np:Assertion .
  
  dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_provenance a np:Provenance .
  
  dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_assertion {
  miriam-gene:6422 a ncit:C16612 .
  
  lld:C1511789 a ncit:C7057 .
  
  dgn-gda:DGN2d5d45dc506616413a7ddb7f642d1c9d sio:SIO_000628 miriam-gene:6422, lld:C1511789;
    a sio:SIO_001121 .
}

dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_provenance {
  dgn-np:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_assertion dcterms:description
      "[Activation of the sonic hedgehog pathway with frequent mutations of the PTCH and SUFU genes, loss of 9q, and positivity for GLI1 and SFRP1 is more frequent in children less than 3 years old and in adults, commonly associated with desmoplastic histology.]. 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:22027544;
    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:NP814825.RAbvHuj63Wzd346f82mZFlYUI50DwpyO93zUyBClc7jIc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:19+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" .
}