@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw> .
@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:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_head {
  this: np:hasAssertion dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_assertion;
    np:hasProvenance dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_provenance;
    np:hasPublicationInfo dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_assertion a np:Assertion .
  
  dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_provenance a np:Provenance .
  
  dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_assertion {
  miriam-gene:57026 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN2f4c7e474401e363a54b6e9d8493e742 sio:SIO_000628 miriam-gene:57026, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_provenance {
  dgn-np:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_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-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:NP556246.RAG7qk4MODKu4VDD-VNCfJGSxRrt9PiX-gerr7tv5nYSw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}