@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I> .
@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:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_head {
  this: np:hasAssertion dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_assertion;
    np:hasProvenance dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_provenance;
    np:hasPublicationInfo dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_assertion a np:Assertion .
  
  dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_provenance a np:Provenance .
  
  dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0598608 a ncit:C7057 .
  
  dgn-gda:DGN8c792c53c4c73cd243e889130edd0eb5 sio:SIO_000628 miriam-gene:4524, lld:C0598608;
    a sio:SIO_001122 .
}

dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_provenance {
  dgn-np:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_assertion dcterms:description
      "[We conclude that after folic acid fortification in the US, measurement of tHcy rather than genotyping of MTHFR 677TT should be used as the primary assay for the diagnosis and monitoring of moderate hyperhomocysteinemia.]. 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:19056652;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61493.RABhFetJgYtU-BrscpwaIbA5u5a9pI5KYIk9FPy1F2o2I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}