@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4> .
@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:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_head {
  this: np:hasAssertion dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion;
    np:hasProvenance dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance;
    np:hasPublicationInfo dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion a np:Assertion .
  
  dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance a np:Provenance .
  
  dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion {
  miriam-gene:4709 a ncit:C16612 .
  
  lld:C0011854 a ncit:C7057 .
  
  dgn-gda:DGN193f7e7fdc4eb2d42fb8cd1072039706 sio:SIO_000628 miriam-gene:4709, lld:C0011854;
    a sio:SIO_001121 .
}

dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_provenance {
  dgn-np:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_assertion dcterms:description
      "[The objectives of this study were: to determine plasma total homocysteine tHcy levels and the prevalence of hyperhomocysteinemia in children with type 1 diabetes, to determine correlates of plasma tHcy levels with nutritional factor such as serum folic acid and vitamin B12 levels, genetic factors as methylenetetrahydrofolate reductase MTHFR gene polymorphism (C677T and A1298C), to attempt to identify possible dependencies between tHcy and the degree of metabolic control, the duration of the disease and presence of complications, and also to determine the relationship between other coronary risk factors.]. 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:16401615;
    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:NP177261.RAQcevj5C7yH943HJLtiHXmY7GKq8alf4Jocc439p1pi4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}