@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg> .
@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:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_head {
  this: np:hasAssertion dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion;
    np:hasProvenance dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance;
    np:hasPublicationInfo dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion a np:Assertion .
  
  dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance a np:Provenance .
  
  dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0025284 a ncit:C7057 .
  
  dgn-gda:DGNf1a431e6852f2ad50573062a0826dba0 sio:SIO_000628 miriam-gene:4524, lld:C0025284;
    a sio:SIO_001122 .
}

dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance {
  dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion dcterms:description
      "[In spite of the established effect of the MTHFR 677 TT genotype on DNA hypomethylation with concomitant inadequate folate levels, the MTHFR 677 TT genotype is not associated with individual susceptibility to HGG.]. 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:16821630;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:30+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" .
}