@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE> .
@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:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_head {
  this: np:hasAssertion dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion;
    np:hasProvenance dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance;
    np:hasPublicationInfo dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion a np:Assertion .
  
  dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance a np:Provenance .
  
  dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN59c4677b78fa6ba7dfec532833606cd2 sio:SIO_000628 miriam-gene:4360, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_provenance {
  dgn-np:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_assertion dcterms:description
      "[To detect hereditary non-polyposis colorectal cancer (HNPCC) patients with a strategy combining clinical selection (patient age at onset of cancer less than 50 years or family history of HNPCC tumors) and microsatellite instability typing plus immunohistochemistry, leading to mismatch repair (MMR) germline 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:16142001;
    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:NP189069.RAAktpjXb7v1G2lSai7tP8yaWc6h1X5sv0TohUWIgnRoE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}