@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs> .
@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:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_head {
  this: np:hasAssertion dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_assertion;
    np:hasProvenance dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_provenance;
    np:hasPublicationInfo dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_assertion a np:Assertion .
  
  dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_provenance a np:Provenance .
  
  dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_assertion {
  miriam-gene:2158 a ncit:C16612 .
  
  lld:C0004779 a ncit:C7057 .
  
  dgn-gda:DGN960d585a3aa3007431d14054d8d96442 sio:SIO_000628 miriam-gene:2158, lld:C0004779;
    a sio:SIO_001121 .
}

dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_provenance {
  dgn-np:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_assertion dcterms:description
      "[Mutations in PATCHED (PTC), the human homolog of the Drosophila patched gene, have been identified in most exons of the gene in patients with the basal cell nevus syndrome and in sporadic basal cell carcinomas.]. 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:9620294;
    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:NP242979.RAylSeDUy87nrokmSAzizGezfyCi9dBCQn6xgg1FiLJgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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" .
}