@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4> .
@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:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_head {
  this: np:hasAssertion dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_assertion ;
    np:hasProvenance dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_provenance ;
    np:hasPublicationInfo dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_assertion a np:Assertion .
  dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_provenance a np:Provenance .
  dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  lld:C0080178 a ncit:C7057 .
  dgn-gda:DGN7f5696bfecb7845e30cc40a4be44031e sio:SIO_000628 miriam-gene:4548 , lld:C0080178 ;
    a sio:SIO_001121 .
}
dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_provenance {
  dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_assertion dcterms:description "[We evaluated the association of polymorphisms of three genes affecting vitamin B12-dependent remethylation of homocysteine, transcobalamin (TC), methionine synthase (MTR) and MTR reductase (MTRR), combined or not with methylenetetrahydrofolate reductase (MTHFR), with the risk of having neural tube defect in 40 children with spina bifida and 58 matched controls from South Italy.]. 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:12812837 ;
    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 ;
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dgn-np:NP758221.RAo4VkYIAYS4LmEg38d218jkNpwzFNllO2i3LHyTANUF4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:39+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> ;
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