@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM> .
@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:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_head {
  this: np:hasAssertion dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion;
    np:hasProvenance dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance;
    np:hasPublicationInfo dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion a np:Assertion .
  
  dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance a np:Provenance .
  
  dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0028960 a ncit:C7057 .
  
  dgn-gda:DGN4803d4a7b8007527975490bf140bbca2 sio:SIO_000628 miriam-gene:4524, lld:C0028960;
    a sio:SIO_001121 .
}

dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance {
  dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion dcterms:description
      "[The objective of this study was to analyze the distribution of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in idiopathic infertile Brazilian patients with nonobstructive azoospermia (NOA) or severe oligozoospermia and fertile Brazilian men as controls to explore the possible association of these polymorphisms and male infertility.]. 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:21138341;
    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:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}