@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_head {
  this: np:hasAssertion dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_assertion;
    np:hasProvenance dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_provenance;
    np:hasPublicationInfo dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_assertion a np:Assertion .
  
  dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_provenance a np:Provenance .
  
  dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN7acd5c1f407782b6eb6c1485fec86c92 sio:SIO_000628 miriam-gene:4524, lld:C0013080;
    a sio:SIO_001122 .
}

dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_provenance {
  dgn-np:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_assertion dcterms:description
      "[Since plasma Hcy may be influenced by genetic polymorphisms, we evaluated the influence of C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR), of A2756G polymorphism in the methionine synthase gene (MTR), and of A80G polymorphism in the reduced folate carrier 1 gene on Hcy concentrations in Brazilian DS patients.]. 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:18060320;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP115984.RAxsdiPEWspMsWEm7zeduv6zeCMFNvJowE_ehpuZRgTzs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:40+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}