@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw> .
@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:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_head {
  this: np:hasAssertion dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_assertion ;
    np:hasProvenance dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_provenance ;
    np:hasPublicationInfo dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_assertion a np:Assertion .
  dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_provenance a np:Provenance .
  dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_assertion {
  miriam-gene:4306 a ncit:C16612 .
  lld:C0596263 a ncit:C7057 .
  dgn-gda:DGNd3e6fc436973c2f7bc8109a7429d6b3a sio:SIO_000628 miriam-gene:4306 , lld:C0596263 ;
    a sio:SIO_001121 .
}
dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_provenance {
  dgn-np:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_assertion dcterms:description "[Since the occurrence of an APC mutation is considered an early event in colorectal carcinogenesis, our findings indicating an extremely low frequency of such changes in and around the MCR suggest that carcinomas of the small intestine arise via a genetic pathway distinct from that involved in the development of carcinomas of the colorectum.]. 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:9033644 ;
    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:NP570474.RAu_6_xesL11PM9txQwYF652w9897dTMY-xgQ0o00DzFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:44+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" .
}