@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY> .
@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:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_head {
  this: np:hasAssertion dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion;
    np:hasProvenance dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance;
    np:hasPublicationInfo dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion a np:Assertion .
  
  dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance a np:Provenance .
  
  dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion {
  miriam-gene:4318 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN7a34091d3777a4dc1a3bc2532bab8744 sio:SIO_000628 miriam-gene:4318, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance {
  dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion dcterms:description
      "[Our results indicate that MMP-2 -1306 C/T polymorphism may be associated with genetic susceptibility to colorectal cancer and the invasive capability of colorectal cancer in Chinese patients. And it is easier for the CC genotype cancer to invade through bowel wall.]. 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:16456793;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}