@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo> .
@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:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_head {
  this: np:hasAssertion dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_assertion;
    np:hasProvenance dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_provenance;
    np:hasPublicationInfo dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_assertion a np:Assertion .
  
  dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_provenance a np:Provenance .
  
  dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN80b8c88f62b65a2b3d1d3c769c3fc6bc sio:SIO_000628 miriam-gene:4292, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_provenance {
  dgn-np:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_assertion dcterms:description
      "[Then, 32 CRC or hereditary nonpolyposis colorectal cancer (HNPCC) patients with family history and 20 cases of sporadic CRC were applied to investigate for the large fragment aberrations of MSH2 and MLH1 genes.]. 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:16331552;
    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:NP208601.RAbOga8rJeFbzMJUP2mzO1d0kLYVTTCpw6wznOb5uuMJo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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" .
}