@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI> .
@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:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_head {
  this: np:hasAssertion dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_assertion ;
    np:hasProvenance dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_provenance ;
    np:hasPublicationInfo dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_provenance a np:Provenance .
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}
dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_assertion {
  miriam-gene:6948 a ncit:C16612 .
  lld:C1140680 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_provenance {
  dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_assertion dcterms:description "[Using PCR-RFLP and HRM analyses, we studied the distribution of BHMT (rs3733890), MTHFD1 (rs2236225), MTHFR (rs1801133), MTR (rs1805087), MTRR (rs1801394) and TCN2 (rs1801198) genotypes and alleles in patients with ovarian cancer (n = 136) and controls (n = 160).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP411673.RAUHwjv5OGPlU3N_pcSS2_Wp3vBAiD6zjwh726VAiKBOI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:04+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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