@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0> .
@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:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_head {
  this: np:hasAssertion dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_assertion;
    np:hasProvenance dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_provenance;
    np:hasPublicationInfo dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_assertion a np:Assertion .
  
  dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_provenance a np:Provenance .
  
  dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_assertion {
  miriam-gene:5624 a ncit:C16612 .
  
  lld:C0007102 a ncit:C7057 .
  
  dgn-gda:DGN99e1082b5a4102f87558993b7a6d86c0 sio:SIO_000628 miriam-gene:5624, lld:C0007102;
    a sio:SIO_001121 .
}

dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_provenance {
  dgn-np:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_assertion dcterms:description
      "[Molecular genetics has identified some inherited mutations (such as at APC and the mismatch repair loci) that predispose to colon cancer and some somatic mutations (such as at APC and p53) that cause sporadic colon tumours.]. 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:9156280;
    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:NP235585.RAlDzD0ruL4eqJdtb3CZi6PJd7_9JXFqE3e9_I7xPQhW0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}