@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A> .
@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:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_head {
  this: np:hasAssertion dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_assertion ;
    np:hasProvenance dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_provenance ;
    np:hasPublicationInfo dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_provenance a np:Provenance .
  dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_assertion {
  miriam-gene:4552 a ncit:C16612 .
  lld:C0007847 a ncit:C7057 .
  dgn-gda:DGNf30b47f51a71fa67de5480ed8688245a sio:SIO_000628 miriam-gene:4552 , lld:C0007847 ;
    a sio:SIO_001121 .
}
dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_provenance {
  dgn-np:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_assertion dcterms:description "[Employing PCR-RFLPs and HRM analyses, we examined the prevalence of BHMT Arg239Gln (rs3733890), MTR Asp919Gly (rs1805087), MTHFR Ala222Val (rs1801133), MTHFD1 Arg653Gln (rs2236225) and MTRR Ile22Met (rs1801394) genotypes and alleles in patients with advanced cervical cancer (n=124) and controls (n=168).]. 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:21349258 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP717911.RAz3QSzrFur8K5q8fnMNe59KvDwPjZLaLEVDh0EaJiF1A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:16+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> ;
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}