@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc> .
@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:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_head {
  this: np:hasAssertion dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_assertion;
    np:hasProvenance dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_provenance;
    np:hasPublicationInfo dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_assertion a np:Assertion .
  
  dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_provenance a np:Provenance .
  
  dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  
  lld:C1708604 a ncit:C7057 .
  
  dgn-gda:DGN6e028b2da571e76ea6794855ded6b4a8 sio:SIO_000628 miriam-gene:5727, lld:C1708604;
    a sio:SIO_001121 .
}

dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_provenance {
  dgn-np:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_assertion dcterms:description
      "[DNA was isolated from both odontogenic keratocyst tissue and peripheral blood of five patients with syndrome and one patient with only multiple odontogenic keratocysts, and mutational analysis of the PTCH gene performed by direct sequencing after amplification of all 23 exons by polymerase chain reaction (PCR).]. 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:18302678;
    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:NP900662.RAs2wpq-LRIQyausTSQAbzTERFnV4xXki-648naWsdmIc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}