@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A> .
@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:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_head {
  this: np:hasAssertion dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_assertion;
    np:hasProvenance dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_provenance;
    np:hasPublicationInfo dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_assertion a np:Assertion .
  
  dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_provenance a np:Provenance .
  
  dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNe156bb90c49373648bcb1985c8f6d610 sio:SIO_000628 miriam-gene:4548, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_provenance {
  dgn-np:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_assertion dcterms:description
      "[We analysed common genetic polymorphisms of 5,10-methylenetetrahydrofolate reductase (MTHFR), thymidylate synthase (TS), methionine synthase (MS) and methionine synthase reductase (MTRR) in 68 children with ALL and 258 healthy controls to investigate their influence on the risk for ALL.]. 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:17454638;
    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:NP917213.RAMVSOZE0KAth9Yu1TqxiEt5EwJu2e5J_2WGcGCZMpE2A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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" .
}