@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU> .
@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:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_head {
  this: np:hasAssertion dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_assertion;
    np:hasProvenance dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_provenance;
    np:hasPublicationInfo dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_assertion a np:Assertion .
  
  dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_provenance a np:Provenance .
  
  dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_assertion {
  miriam-gene:4163 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGN53371dcc543efcb6c4b25483072fa5ce sio:SIO_000628 miriam-gene:4163, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_provenance {
  dgn-np:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_assertion dcterms:description
      "[Linkage analysis shows that these susceptibility genes are different from the mouse homologs of the genes known to be somatically mutated in human colon cancer (KRAS2, TP53, DCC, MCC, APC, MSH2, and probably also MLH1).]. 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:8577718;
    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:NP632765.RAFeZ6WKGzwEz0abSfDz3oW-LRegGD_cprVLxUScg_ynU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:22+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}