@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ> .
@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:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_head {
  this: np:hasAssertion dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_assertion;
    np:hasProvenance dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_provenance;
    np:hasPublicationInfo dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_assertion a np:Assertion .
  
  dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_provenance a np:Provenance .
  
  dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0334108 a ncit:C7057 .
  
  dgn-gda:DGNac4d017e7849fd68654f080733ec6008 sio:SIO_000628 miriam-gene:5624, lld:C0334108;
    a sio:SIO_001121 .
}

dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_provenance {
  dgn-np:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_assertion dcterms:description
      "[The findings demonstrate the value of the PTT in identifying mosaic mutations in apparently APC mutation negative FAP patients with de novo classical polyposis and the need to keep the PTT within the diagnostic repertoire for APC mutation analysis.]. 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:21653199;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP900264.RAxONrTBC9wLd0pFf6ZdjpdF6f7gF9SKeDFA7Jag-jggQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:32+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" .
}