@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM> .
@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:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_head {
  this: np:hasAssertion dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_assertion;
    np:hasProvenance dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_provenance;
    np:hasPublicationInfo dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_assertion a np:Assertion .
  
  dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_provenance a np:Provenance .
  
  dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_assertion {
  miriam-gene:1048 a ncit:C16612 .
  
  lld:C2939420 a ncit:C7057 .
  
  dgn-gda:DGN6b32c1d2e78ae12ae7288542a580ef01 sio:SIO_000628 miriam-gene:1048, lld:C2939420;
    a sio:SIO_001121 .
}

dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_provenance {
  dgn-np:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_assertion dcterms:description
      "[MSI-H colon cancers (13%) had distinct phenotypes including young age at diagnosis, family history of colorectal cancer, early Tumor, Node, Metastasis (TNM) stage, proximal location, poor differentiation, and high level of baseline carcinoembryonic antigen (CEA), while MSI-H rectal cancers (4.3%) showed similar clinicopathological characteristics to MSS/MSI-L tumours except for family history of colorectal cancer.]. 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:22071131;
    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:NP335419.RADDO7lLgVTUMyYX8bvZr-slmdnUS5M8hWJ6novKnoUJM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}