@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U> .
@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:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_head {
   this: np:hasAssertion dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_assertion ;
    np:hasProvenance dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_provenance ;
    np:hasPublicationInfo dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_assertion a np:Assertion .
  dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_provenance a np:Provenance .
  dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_assertion {
   miriam-gene:875 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGNb39132fa94c210cb7d9b6859c9fee3d4 sio:SIO_000628 miriam-gene:875 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_provenance {
   dgn-np:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_assertion dcterms:description "[In a group of 121 case families (mother, father, and proband with DS and AVSD) and 122 control families (mother, father, and proband with DS and no CHD), tag SNPs were genotyped in and around five folate pathway genes: 5,10-methylenetetrahyrdofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), cystathionine beta-synthase (CBS), and the reduced folate carrier (SLC19A1, RFC1).]. 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:20718043 ;
    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:NP276227.RALdh03MJhLaL5aSIxYgZxogbw8JLHoPlh93ZAThJKs1U130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:35+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" .
}