@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU> .
@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:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_head {
  this: np:hasAssertion dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_assertion;
    np:hasProvenance dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_provenance;
    np:hasPublicationInfo dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_assertion a np:Assertion .
  
  dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_provenance a np:Provenance .
  
  dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0001430 a ncit:C7057 .
  
  dgn-gda:DGNb7327a2ff3bcf411af5c808d598dfc5f sio:SIO_000628 miriam-gene:4595, lld:C0001430;
    a sio:SIO_001121 .
}

dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_provenance {
  dgn-np:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_assertion dcterms:description
      "[To examine the relationship between monoallelic MYH variants and susceptibility to sporadic colorectal cancer (CRC), 92 cases of sporadic CRC, 19 cases of familial CRC not meeting the Bethesda guidelines, 17 cases with multiple adenomas, and 53 normal blood donors were screened for 8 potentially pathogenic germ-line MYH variants.]. 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:15034862;
    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:NP436569.RAP2EudSiKt_DOEu3h0cDPCgdiXx7GfSV5XipQtsCYykU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:03+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" .
}