@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo> .
@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:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_head {
   this: np:hasAssertion dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_assertion ;
    np:hasProvenance dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_provenance ;
    np:hasPublicationInfo dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_provenance a np:Provenance .
  dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0338656 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_provenance {
   dgn-np:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_assertion dcterms:description "[To elucidate the specific role of the TT genotype of MTHFR in the development of cerebral infarction with and without cognitive impairment, we determined the prevalence of hyperhomocyst(e)inemia and the C677T genotypes of MTHFR in 143 patients with vascular dementia, 122 patients with cerebral infarction, and 217 healthy subjects matched for age and sex.]. 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:10938012 ;
    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:NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:24+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 ;
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}