@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I> .
@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:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_head {
  this: np:hasAssertion dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_assertion;
    np:hasProvenance dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_provenance;
    np:hasPublicationInfo dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_assertion a np:Assertion .
  
  dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_provenance a np:Provenance .
  
  dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0598608 a ncit:C7057 .
  
  dgn-gda:DGN181e2eb6b024faa3da8da1f018734847 sio:SIO_000628 miriam-gene:4524, lld:C0598608;
    a sio:SIO_001121 .
}

dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_provenance {
  dgn-np:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_assertion dcterms:description
      "[Although it is accepted that moderate hyperhomocysteinemia significantly increases the risk for coronary, cerebrovascular, and peripheral vascular diseases, our data suggest that a mutation of the MTHFR gene, which has been associated with a thermolabile form of the enzyme and with hyperhomocysteinemia in subjects with plasma folate below the median, does not appear to be significantly associated with risk for premature coronary artery disease or for restenosis after coronary angioplasty.]. 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:8994411;
    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:NP1365624.RAhtD5KnRij47ERVqkAmYP18b8Ho4aj05MTtsdOGTPr8I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:05+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" .
}