@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes> .
@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:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_head {
  this: np:hasAssertion dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion;
    np:hasProvenance dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance;
    np:hasPublicationInfo dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion a np:Assertion .
  
  dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance a np:Provenance .
  
  dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN5fb09c8e98c7255c016a73a64ec58779 sio:SIO_000628 miriam-gene:5624, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance {
  dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion dcterms:description
      "[Analyses included completion of APC gene exon 16 sequencing, analysis for APC gene copy number variations (deletions or duplications), MUTYH gene sequencing, and microsatellite instability in CRC patients fulfilling Bethesda (laboratory investigation) criteria for Lynch syndrome.]. 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:21287799;
    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:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:18+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" .
}