@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU> .
@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:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_head {
  this: np:hasAssertion dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_assertion;
    np:hasProvenance dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_provenance;
    np:hasPublicationInfo dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_assertion a np:Assertion .
  
  dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_provenance a np:Provenance .
  
  dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGNb31897763678d70dd4b218fbf878f761 sio:SIO_000628 miriam-gene:5624, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_provenance {
  dgn-np:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_assertion dcterms:description
      "[Many cases of HNPCC are due to germline mutations in DNA mismatch repair genes, leading to the tumor phenotype of microsatellite instability (MSI), and most cases of FAP are caused by germline APC mutations.]. 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:11135435;
    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:NP304179.RALcjZRWIrEwFpM1jIdDvRIBLDuo871zVKa1uudstWgNU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:03+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" .
}