@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw> .
@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:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_head {
  this: np:hasAssertion dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_assertion;
    np:hasProvenance dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_provenance;
    np:hasPublicationInfo dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_assertion a np:Assertion .
  
  dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_provenance a np:Provenance .
  
  dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_assertion {
  miriam-gene:2352 a ncit:C16612 .
  
  lld:C0025312 a ncit:C7057 .
  
  dgn-gda:DGNcdfe39ba86bbdb03372156a4acf8eae2 sio:SIO_000628 miriam-gene:2352, lld:C0025312;
    a sio:SIO_001121 .
}

dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_provenance {
  dgn-np:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_assertion dcterms:description
      "[This study used the SNPlex Genotyping (ABI, Foster City, CA) platform to genotype 20 single polymorphic variants across the folate receptor genes (FOLR1, FOLR2, FOLR3) and the folate carrier gene (SLC19A1) to assess their association to MM.]. 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:20683905;
    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:NP454832.RAXMdL2ibvN7M8_8B8hRqL9Gr03KkTQ_K091MrQuHjmFw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:31+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" .
}