@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA> .
@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:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_head {
  this: np:hasAssertion dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion;
    np:hasProvenance dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance;
    np:hasPublicationInfo dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion a np:Assertion .
  
  dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance a np:Provenance .
  
  dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN3c5ef13610a3b4c45f4c227daa71504e sio:SIO_000628 miriam-gene:4360, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance {
  dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion dcterms:description
      "[We examined the validity of immunohistochemistry for mismatch repair (MMR) proteins in colorectal cancer specimens to identify patients at risk for Lynch syndrome (hereditary nonpolyposis colorectal cancer) and patients with sporadic microsatellite instable colorectal cancer.]. 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:18677806;
    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:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}