@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg> .
@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:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_head {
  this: np:hasAssertion dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion;
    np:hasProvenance dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance;
    np:hasPublicationInfo dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion a np:Assertion .
  
  dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance a np:Provenance .
  
  dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN9434acaea1126724a70ddfe657bd0dc0 sio:SIO_000628 miriam-gene:4548, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance {
  dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion dcterms:description
      "[The single nucleotide polymorphisms, MTHFR C677T, A1298C, MTR A2756G and MTRR A66G, cause alteration in the homocysteine levels and reduced enzymatic activity that generates deficiency in the assimilation of folates associated with DNA damage; that is, why it is important to know if the single nucleotide polymorphisms are associated with the pathological characteristics and development of prostate cancer, through a case-control retrospective study.]. 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:23459165;
    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:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}