@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI> .
@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:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_head {
  this: np:hasAssertion dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion;
    np:hasProvenance dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance;
    np:hasPublicationInfo dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion a np:Assertion .
  
  dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance a np:Provenance .
  
  dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNddabf409515e41f86a693fd3e9810e69 sio:SIO_000628 miriam-gene:4524, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance {
  dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion dcterms:description
      "[This study points out the importance of the interactions between the MTHFR C677T, MTHFR A1298C and MTR A2756G polymorphisms, and also highlights the relevance of the MTR A2756G polymorphism and age in breast cancer risk.]. 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:23155246;
    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:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}