@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_head {
  this: np:hasAssertion dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_assertion;
    np:hasProvenance dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_provenance;
    np:hasPublicationInfo dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_assertion a np:Assertion .
  
  dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_provenance a np:Provenance .
  
  dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_assertion {
  miriam-gene:6948 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNe636d987b2cbe4d4c22f3c7ec6b44d38 sio:SIO_000628 miriam-gene:6948, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_provenance {
  dgn-np:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_assertion dcterms:description
      "[We examined five sequence variants, i.e., I23V, G94S, P259R, S348F, and R399Q, in the TC gene as possible determinants of tHcy and, concordantly, as possible risk factors for CVD in 190 vascular disease patients and 601 controls.]. 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:12194912;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP726229.RAtHHZkC5jLBIvkEuqMrfq8ffWgPVgtrQDMHNetDZO074130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:58+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:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}