@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_head {
  this: np:hasAssertion dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion;
    np:hasProvenance dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance;
    np:hasPublicationInfo dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion a np:Assertion .
  
  dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance a np:Provenance .
  
  dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN2f765f98e72d15bb836c5373d8bc5a07 sio:SIO_000628 miriam-gene:4360, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance {
  dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion dcterms:description
      "[We investigated 96 colorectal carcinomas, 58 gastric carcinomas and 41 endometrial carcinomas, occurring as part of inherited DNA mismatch repair (MMR) deficiency (Lynch syndrome), familial colorectal carcinoma without MMR gene mutations or sporadically.]. 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:21327300;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}