@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE> .
@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:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_head {
  this: np:hasAssertion dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_assertion;
    np:hasProvenance dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_provenance;
    np:hasPublicationInfo dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_assertion a np:Assertion .
  
  dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_provenance a np:Provenance .
  
  dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGNedd4cf7e06796eabdafd10b966606d5f sio:SIO_000628 miriam-gene:4595, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_provenance {
  dgn-np:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_assertion dcterms:description
      "[Approximately 69% of the excess familial risk in FDRs can be ascribed to MSS CRC, and although the pattern of familial risk supports recessive susceptibility in addition to MUTYH, the absolute risk of CRC is at best modest.]. 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:19307499;
    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:NP262338.RA2xY6Q-oe7AZ2CF-8gf8uCon-EVRtJm8o8BZnVvNNgwE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}