@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4> .
@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 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:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_head {
  this: np:hasAssertion dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_assertion;
    np:hasProvenance dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_provenance;
    np:hasPublicationInfo dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_assertion a np:Assertion .
  
  dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_provenance a np:Provenance .
  
  dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_assertion {
  miriam-gene:2651 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN361875ee01ac9efa6ab98a54347cb8ed sio:SIO_000628 miriam-gene:2651, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_provenance {
  dgn-np:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_assertion dcterms:description
      "[Molecular genetic findings have enabled hereditary CRC to be divided into two groups: (1) tumours that show microsatellite instability (MSI), occur more frequently in the right colon, have diploid DNA, harbour characteristic mutations such as transforming growth factor beta type II receptor and BAX, and behave indolently, of which HNPCC is an example; and (2) tumours with chromosomal instability (CIN), which tend to be left sided, show aneuploid DNA, harbour characteristic mutations such as K-ras, APC, and p53, and behave aggressively, of which FAP is an example.]. 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:10544223;
    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:NP266602.RA_n5rypIMCMvx_0CRyu7qqzxYZyl12y5jiTPjx0GiAV4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:46+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" .
}