@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s> .
@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:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_head {
  this: np:hasAssertion dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_assertion ;
    np:hasProvenance dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_provenance ;
    np:hasPublicationInfo dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_assertion a np:Assertion .
  dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_provenance a np:Provenance .
  dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_assertion {
  miriam-gene:1559 a ncit:C16612 .
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dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_provenance {
  dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_assertion dcterms:description "[In conclusion, CYP2C9*2 or *3 compound heterozygotes and homozygotes have low warfarin requirements even after excluding liver disease, excessive alcohol or acetaminophen consumption, low body weight, advancing age, and drug interactions. These polymorphisms increase the rate of excessive anticoagulation, but this risk does not appear to be associated with higher bleeding rates when anticoagulation status is closely monitored.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
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}
dgn-np:NP45770.RA7jkHYmb2KKZST2eNgmsi52A6MnCpnblg0HghRFlX60s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}