@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg> .
@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:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_head {
  this: np:hasAssertion dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion;
    np:hasProvenance dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance;
    np:hasPublicationInfo dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion a np:Assertion .
  
  dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance a np:Provenance .
  
  dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN0beca3edad023b594e10ce2af6254db5 sio:SIO_000628 miriam-gene:4292, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_provenance {
  dgn-np:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_assertion dcterms:description
      "[Germline mutations or the malfunctioning of postreplicative mismatch repair genes (MMR) are responsible of hereditary nonpolyposis colorectal cancer (HNPCC), and are also implied in some sporadic colorectal cancer (CRC) forms without any familial history of this disease.]. 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:19665066;
    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:NP54655.RAnvq62DwcqQNFMaoMAr33PXIXE6N478_mpI_SReoLCMg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}