@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es> .
@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:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_head {
  this: np:hasAssertion dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion;
    np:hasProvenance dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance;
    np:hasPublicationInfo dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion a np:Assertion .
  
  dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance a np:Provenance .
  
  dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C1458155 a ncit:C7057 .
  
  dgn-gda:DGN0bc9a3acded6075043e1e9a72769e1a7 sio:SIO_000628 miriam-gene:4524, lld:C1458155;
    a sio:SIO_001121 .
}

dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance {
  dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion dcterms:description
      "[To evaluate the C677T and A1298C functional polymorphisms in the MTHFR gene and their associations with breast cancer risk, as well as the potential modifying effect by plasma folate status on the MTHFR-associated risk, a hospital-based case-control study was conducted on a Taiwanese population consisting of 146 histologically confirmed incident breast cancer cases and their 285 age-matched controls without a history of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:16777985;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:09+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" .
}