@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw> .
@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:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_head {
  this: np:hasAssertion dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_assertion;
    np:hasProvenance dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_provenance;
    np:hasPublicationInfo dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_assertion a np:Assertion .
  
  dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_provenance a np:Provenance .
  
  dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGNb0884c866fb8f2fa17d1abcd39392594 sio:SIO_000628 miriam-gene:4524, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_provenance {
  dgn-np:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_assertion dcterms:description
      "[Our data indicate that the C677T MTHFR polymorphism does not significantly contribute to the inherited genetic susceptibility to breast and prostate cancer, while we show some evidence for possible genetic contribution of this polymorphism to the development of head and neck carcinoma.]. 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:17573062;
    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:NP228386.RACdFbNHdbdl6js217RKKbBq7rSfi87GsGvKAayBSpZnw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}