@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY> .
@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:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_head {
  this: np:hasAssertion dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_assertion;
    np:hasProvenance dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_provenance;
    np:hasPublicationInfo dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_assertion a np:Assertion .
  
  dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_provenance a np:Provenance .
  
  dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_assertion {
  miriam-gene:5395 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN34473f1fc0ea4c289b6bee57c53a4730 sio:SIO_000628 miriam-gene:5395, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_provenance {
  dgn-np:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_assertion dcterms:description
      "[Patients (n = 112) from 285 families who were counseled between 1990 and 2005 at a clinic for patients at high risk for HNPCC were selected for screening to detect mutations in MMR genes MLH1, MSH2, MSH6, and PMS2 based on family history, microsatellite instability (MSI), and immunohistochemical analysis of MMR protein expression.]. 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:17312306;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62629.RAb4vx0CZTzOVRigpZW_4tOqp6uZrJNfnqm0Sq09Mv9GY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}