@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_head {
  this: np:hasAssertion dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_assertion ;
    np:hasProvenance dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_provenance ;
    np:hasPublicationInfo dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_assertion a np:Assertion .
  dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_provenance a np:Provenance .
  dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  lld:C0021390 a ncit:C7057 .
  dgn-gda:DGNc043d2a5dedecc82219d88cf2b2162d0 sio:SIO_000628 miriam-gene:4524 , lld:C0021390 ;
    a sio:SIO_001122 .
}
dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_provenance {
  dgn-np:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_assertion dcterms:description "[No significant difference was found between IBD patients and controls with regard to the prevalence of homozygotes for the C677T variant (TT) of MTHFR or the prevalence of heterozygotes for the CBS-gene mutation (IN).]. 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:11569694 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP574909.RAuVamww0tyTd3rUDyTn_d_nF0rADXHybnjLYEiXVepGY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:22+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}