@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w> .
@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:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_head {
  this: np:hasAssertion dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_assertion;
    np:hasProvenance dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_provenance;
    np:hasPublicationInfo dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_assertion a np:Assertion .
  
  dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_provenance a np:Provenance .
  
  dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_assertion {
  miriam-gene:2155 a ncit:C16612 .
  
  lld:C0151744 a ncit:C7057 .
  
  dgn-gda:DGNb6d61f3ffefe0a65d60ad6ed5b138bd9 sio:SIO_000628 miriam-gene:2155, lld:C0151744;
    a sio:SIO_001121 .
}

dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_provenance {
  dgn-np:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_assertion dcterms:description
      "[Interestingly, lowering the plasma levels of FVII with low dose warfarin to the same low normal range as that associated with the 'protective' genotypes, results in protection against ischaemic heart disease, reducing mortality in high risk men.]. 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:10878696;
    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:NP672702.RAm7tzBgDivLTj5cyEfLxwfgKyvOgpXAV2affHy3M_T9w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:46+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" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}