@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_head {
  this: np:hasAssertion dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_assertion;
    np:hasProvenance dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_provenance;
    np:hasPublicationInfo dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_assertion a np:Assertion .
  
  dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_provenance a np:Provenance .
  
  dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN7975cc0188c094f7c91166e483d0fbad sio:SIO_000628 miriam-gene:4436, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_provenance {
  dgn-np:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_assertion dcterms:description
      "[Hereditary non-polyposis colorectal cancer (HNPCC or Lynch syndrome) is characterized by early occurrence of colorectal malignancies, localization of tumors in the proximal colon, frequency of multiple primaries (both synchronous and metachronous) and an autosomal dominant type of genetic transmission.]. 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:8644370;
    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:NP1350786.RAS8sibGLF2v72NXbBMyWgSQm6H562oGXrclve3RYGlH0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:58+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" .
}