@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI> .
@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:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_head {
  this: np:hasAssertion dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion;
    np:hasProvenance dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance;
    np:hasPublicationInfo dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion a np:Assertion .
  
  dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance a np:Provenance .
  
  dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion {
  miriam-gene:4709 a ncit:C16612 .
  
  lld:C3495426 a ncit:C7057 .
  
  dgn-gda:DGN3d1ac43b35aa561eb4f506a363149e75 sio:SIO_000628 miriam-gene:4709, lld:C3495426;
    a sio:SIO_001121 .
}

dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_provenance {
  dgn-np:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_assertion dcterms:description
      "[Plasma Hcy levels, MTHFR gene mutation, red blood cell (RBC) folate and vitamin B12 serum levels were measured in all subjects.Results: No significant differences were observed neither in plasma Hcy levels, RBC folate and vitamin B12 serum levels nor in the prevalence of homozygous and heterozygous MTHFR gene mutation between the two groups studied.Conclusions: In the present study RM is not associated with hyperhomocysteinemia, and/or the MTHFR gene mutation.]. 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:23095199;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP239416.RA8gP4LeU9WTtXoRF5YzS0ev9QbDL6dMXnzrmccI8S0xI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}