@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA> .
@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:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_head {
  this: np:hasAssertion dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_assertion;
    np:hasProvenance dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_provenance;
    np:hasPublicationInfo dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_assertion a np:Assertion .
  
  dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_provenance a np:Provenance .
  
  dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0206624 a ncit:C7057 .
  
  dgn-gda:DGNcafcce51f6522c2055562668cc8a455d sio:SIO_000628 miriam-gene:324, lld:C0206624;
    a sio:SIO_001121 .
}

dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_provenance {
  dgn-np:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_assertion dcterms:description
      "[Presuming that the HB in the two siblings was the first manifestation of FAP we performed APC mutation analysis in DNA from archived tumour tissue of his sister and in blood samples of both parents.]. 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:22692730;
    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:NP238741.RABr3NnS8115iB3bYcEPa_EtMO2HyYJNYp8HtbKEuEfYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}