@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY> .
@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:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_head {
  this: np:hasAssertion dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_assertion;
    np:hasProvenance dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_provenance;
    np:hasPublicationInfo dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_assertion a np:Assertion .
  
  dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_provenance a np:Provenance .
  
  dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN4804927c0ea335f09e226a1a396780c5 sio:SIO_000628 miriam-gene:4595, lld:C0032580;
    a sio:SIO_001122 .
}

dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_provenance {
  dgn-np:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_assertion dcterms:description
      "[The lack of complementation of the hMYH variants for MutY, and the reduced activity of the Y82C and G253D E.coli enzymes, provide additional circumstantial evidence that the somatic mutations in APC, and the occurrence of FAP in Family N, are due to a reduced ability of the Y165C and G382D hMYH enzymes to recognize and repair OG:A mismatches.]. 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:12628248;
    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:NP386402.RAVpJ5dvVA15-JQ8IHxCuHn365eJg6dsz_5YT1NHQgmPY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:40+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" .
}