@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0> .
@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 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:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_head {
  this: np:hasAssertion dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_assertion;
    np:hasProvenance dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_provenance;
    np:hasPublicationInfo dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_assertion a np:Assertion .
  
  dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_provenance a np:Provenance .
  
  dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN33f3ae6a79a76a21c57afe85a8a73a45 sio:SIO_000628 miriam-gene:3265, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_provenance {
  dgn-np:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_assertion dct:description
      "[ APC-I1307K, HRAS1-VNTR, and MTHFR variants represent the strongest candidates for low penetrance susceptibility alleles identified to date. Although their genotypic risks are modest, their high frequency in the population implies that they may well have considerable impact on colorectal cancer incidence. Determining precise risk estimates associated with other variants and gene-gene and gene-environment interactions will be contingent on further studies with sample sizes larger than typically used to date.]. 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:11487538;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57549.RAxulB1lN2To1ZRadiLssqpcc5SNdnd8mNRTZkp8s79U0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}