@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ> .
@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/v4.0.0/void/> .

dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_head {
  this: np:hasAssertion dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_assertion;
    np:hasProvenance dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_provenance;
    np:hasPublicationInfo dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_assertion a np:Assertion .
  
  dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_provenance a np:Provenance .
  
  dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGN438a3217349faaab1a887fa451f12846 sio:SIO_000628 miriam-gene:4524, lld:C0011849;
    a sio:SIO_001122 .
}

dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_provenance {
  dgn-np:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_assertion dcterms:description
      "[The Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is associated with various diseases (vascular, cancers, neurology, diabetes, psoriasis, etc) with the epidemiology of the polymorphism of the C677T that varies dependent on the geography and ethnicity.]. 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:25449138;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1242414.RAl1DSO0nVUmHrAQTY70eokVNhoSiwH3KbDOblVMRgNsQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:09+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}