@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w> .
@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/v3.0.0/void/> .

dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_head {
  this: np:hasAssertion dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_assertion;
    np:hasProvenance dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_provenance;
    np:hasPublicationInfo dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_assertion a np:Assertion .
  
  dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_provenance a np:Provenance .
  
  dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0025149 a ncit:C7057 .
  
  dgn-gda:DGN8c4910d44cbbdfc190508664fc6fa0cc sio:SIO_000628 miriam-gene:5624, lld:C0025149;
    a sio:SIO_001121 .
}

dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_provenance {
  dgn-np:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_assertion dcterms:description
      "[In patients with FAP and identifiable APC gene mutation, CNS tumors, especially medulloblastoma which developed in most cases during childhood, are more common in females with FAP and APC gene mutation in codons 686-1217.]. 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:17238184;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP648102.RA70bwLygUVfK15aboYjr9a54yRiH4uKHi1LkdbIxzu2w130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:09+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}