@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI> .
@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:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_head {
  this: np:hasAssertion dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_assertion ;
    np:hasProvenance dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_provenance ;
    np:hasPublicationInfo dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_assertion a np:Assertion .
  dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_provenance a np:Provenance .
  dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_assertion {
  miriam-gene:875 a ncit:C16612 .
  lld:C0040038 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_provenance {
  dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_assertion dcterms:description "[The frequency of the heterozygous 844ins68 mutation of the cystathionine beta-synthase (CBS) gene and of its association with the homozygous C677T transition of the methylenetetrahydrofolate reductase (MTHFR) gene, plasma fasting tHcy, folate and vitamin B12 levels were evaluated in 309 consecutive patients with objectively diagnosed early-onset venous (n = 200) or arterial thromboembolic disease (n = 109) recruited over 25 months in Milan (North Italy) and Naples (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:11057853 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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 .
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dgn-np:NP925112.RAXA29YwwEFlRxBwJxEfuDBJgEyi6ByF3DlhAkIf7AVoI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:27+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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