@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E> .
@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:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_head {
  this: np:hasAssertion dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_assertion;
    np:hasProvenance dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_provenance;
    np:hasPublicationInfo dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_assertion a np:Assertion .
  
  dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_provenance a np:Provenance .
  
  dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN9537489aefc4e5387708f70c9e734be4 sio:SIO_000628 miriam-gene:4292, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_provenance {
  dgn-np:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_assertion dcterms:description
      "[The discipline of molecular genetics has identified germline mutations that include APC in familial adenomatous polyposis (FAP) and mutator genes, namely MSH2, MLH1, PMS1, and PMS2 in hereditary nonpolyposis colorectal cancer (HNPCC).]. 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:9062584;
    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:NP276282.RALGQeLwRhccoJ4W1B1zYlB0GyLrzVCpVWmno3xfQBT8E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}