@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ> .
@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:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_head {
  this: np:hasAssertion dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_assertion;
    np:hasProvenance dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_provenance;
    np:hasPublicationInfo dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_assertion a np:Assertion .
  
  dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_provenance a np:Provenance .
  
  dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0001430 a ncit:C7057 .
  
  dgn-gda:DGNa0a006d6be6952638b58b3cb2025986f sio:SIO_000628 miriam-gene:4595, lld:C0001430;
    a sio:SIO_001122 .
}

dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_provenance {
  dgn-np:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_assertion dcterms:description
      "[Here, we describe a screening method, HRM, for the detection of both heterozygous and homozygous mutations in the gene encoding MUTYH in selected samples of patients with phenotype of MAP. We refine the capabilities of HRM-PCR and apply it to a gene not y]. 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:20687945;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP183234.RArFsSUjuRAl13iWidyiMvDIAiOf7nQwMya7ZxcSf7oVQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:10+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" .
}