@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A> .
@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:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_head {
  this: np:hasAssertion dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion;
    np:hasProvenance dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance;
    np:hasPublicationInfo dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion a np:Assertion .
  
  dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance a np:Provenance .
  
  dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN9419ff93deee9e6cf02ba342db8af787 sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance {
  dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion dcterms:description
      "[The discovery that mutations occur with equal frequency in MSS and MSI tumors and are most frequent in MSI tumors lacking MLH1 methylation has implications for Lynch syndrome screening and mutation testing.]. 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:25224212;
    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:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:59+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" .
}