@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
.
lld:C0005779
a
ncit:C7057
.
dgn-gda:DGN04be69ee4b28d8672f440a21b3d265c3
sio:SIO_000628
miriam-gene:1559
,
lld:C0005779
;
a
sio:SIO_001122
.
}
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
;
sio:SIO_000772
miriam-pubmed:15175798
;
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
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
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
;
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" .
}