@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA> .
@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:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_head {
  this: np:hasAssertion dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_assertion ;
    np:hasProvenance dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_provenance ;
    np:hasPublicationInfo dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_assertion a np:Assertion .
  dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_provenance a np:Provenance .
  dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_assertion {
  miriam-gene:4709 a ncit:C16612 .
  lld:C0042847 a ncit:C7057 .
  dgn-gda:DGNab611ee165fa3bd03304da883cb8de1f sio:SIO_000628 miriam-gene:4709 , lld:C0042847 ;
    a sio:SIO_001121 .
}
dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_provenance {
  dgn-np:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_assertion dcterms:description "[In this study, our aim was to investigate the association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism on the vitamin B12 therapy response in 95 patients with vitamin B12 deficiency and 92 healthy control subjects using vitamin B12, plasma total homocysteine (tHcy), and folate as the main measure of outcome.]. 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:22084937 ;
    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:NP188724.RAMXvbGa4nGx9D4fuqoECe3f-og7r9XVI-pzHVl3NE6TA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
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}