@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_head {
  this: np:hasAssertion dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_assertion;
    np:hasProvenance dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_provenance;
    np:hasPublicationInfo dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_assertion a np:Assertion .
  
  dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_provenance a np:Provenance .
  
  dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  
  lld:C2751544 a ncit:C7057 .
  
  dgn-gda:DGNccce89c96a7c1a030242076e4decbb78 sio:SIO_000628 miriam-gene:5727, lld:C2751544;
    a sio:SIO_001122 .
}

dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_provenance {
  dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_assertion dcterms:description
      "[We have screened the 23 PTC exons for mutations using single strand conformation polymorphism analysis of DNA from 86 basal cell nevus syndrome probands, 26 sporadic basal cell carcinomas, and seven basal cell nevus syndrome-associated basal cell carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:9620294;
    prov:wasDerivedFrom dgn-void:uniprot-2016;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}

dgn-np:NP9768.RACMP7jfrXP_B0Tq9wt8xNKLc9F8Sr6cKodJmt9r8yPec130_publicationInfo {
  this: dcterms:created "2016-05-13T12:41:54+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}