@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8> .
@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:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_head {
  this: np:hasAssertion dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_assertion;
    np:hasProvenance dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_provenance;
    np:hasPublicationInfo dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_assertion a np:Assertion .
  
  dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_provenance a np:Provenance .
  
  dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN9e3533e40762b4fed64d84ece15dde94 sio:SIO_000628 miriam-gene:324, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_provenance {
  dgn-np:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_assertion dcterms:description
      "[Because of recent findings that most cases of FAP are due to mutations of the adenomatous polyposis coli gene at chromosome 5q21, genetic testing will probably be incorporated as the first step in the management of individuals at risk for this condition, and screening regimens can be modified.]. 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:8074838;
    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:NP1331381.RA6BsAvZhk5EEIwJr14LDLpMchkQ78EXiLV8E1G6ARSy8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:49+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" .
}