@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_head {
  this: np:hasAssertion dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_assertion;
    np:hasProvenance dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_assertion a np:Assertion .
  
  dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_provenance a np:Provenance .
  
  dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN7a08c342bd21760c28578cc61d7ba8dd sio:SIO_000628 miriam-gene:324, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_provenance {
  dgn-np:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_assertion dcterms:description
      "[Many colorectal cancers (CRCs) develop in genetically susceptible individuals most of whom are not carriers of germ line mismatch repair or APC gene mutations and much of the heritable risk of CRC appears to be attributable to the co-inheritance of multiple low-risk variants.]. 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:22294761;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP957670.RAidkiT9aWPGer8UUvTOFXEf7s0B2sIURCnk3psPbvIUQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:59+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}