@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0> .
@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:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_head {
  this: np:hasAssertion dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion;
    np:hasProvenance dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance;
    np:hasPublicationInfo dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion a np:Assertion .
  
  dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance a np:Provenance .
  
  dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGNc13f82f371b63ef8b098c9f0cc483c74 sio:SIO_000628 miriam-gene:4436, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_provenance {
  dgn-np:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_assertion dcterms:description
      "[A substantial proportion of MLH1 and MSH2 gene mutations in hereditary nonpolyposis colon cancer syndrome (HNPCC) families are characterized by nucleotide substitutions, either within the coding sequence (missense or silent mutations) or in introns.]. 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:16395668;
    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:NP529660.RApD95DQQugjfz6HRKnPtnXXTGy9-GbkHPS2312G34xm0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:44+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" .
}