@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI> .
@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:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_head {
   this: np:hasAssertion dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_assertion ;
    np:hasProvenance dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_provenance ;
    np:hasPublicationInfo dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_assertion a np:Assertion .
  dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_provenance a np:Provenance .
  dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_assertion {
   miriam-gene:4595 a ncit:C16612 .
  lld:C3272841 a ncit:C7057 .
  dgn-gda:DGNe72069df94a1e6a3ebb37732fe93f4e4 sio:SIO_000628 miriam-gene:4595 , lld:C3272841 ;
    a sio:SIO_001122 .
}
dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_provenance {
   dgn-np:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_assertion dcterms:description "[The aim of this study was to assess the frequency of the germline MUTYH mutations p.Y179C and p.G396D in Brazilian patients with MAP and other hereditary colorectal cancer (CRC) phenotypes, as well as in sporadic CRC cases.]. 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:21424714 ;
    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:NP881334.RAoWXHXT7Ce9YKrF7NcqzwvQkkh4hbgNQO19WnEsC0CXI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:24+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" .
}