@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y> .
@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:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_head {
  this: np:hasAssertion dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_assertion;
    np:hasProvenance dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_provenance;
    np:hasPublicationInfo dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_assertion a np:Assertion .
  
  dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_provenance a np:Provenance .
  
  dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGNbe64de47585efe58c679823d17c3525f sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_provenance {
  dgn-np:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_assertion dcterms:description
      "[Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly MLH1, MSH2 and in families with excess endometrial cancer also MSH6.]. 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:14961575;
    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:NP431648.RAieXD8lq4g2BcOqSuxgJi95FC2Ac1TqUeZO9xMLcpE3Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:01+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" .
}