@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0
> .
@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:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_head
{
this:
np:hasAssertion
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion
;
np:hasProvenance
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance
;
np:hasPublicationInfo
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion
a
np:Assertion
.
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance
a
np:Provenance
.
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion
{
miriam-gene:1284
a
ncit:C16612
.
lld:C0232197
a
ncit:C7057
.
dgn-gda:DGN6f0635328b407622397d0c028b0326f3
sio:SIO_000628
miriam-gene:1284
,
lld:C0232197
;
a
sio:SIO_001121
.
}
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_provenance
{
dgn-np:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_assertion
dcterms:description
"[Even if patients undergo screening with MRI as well as genotyping, currently available data on the role of MRI on risk of ICH and warfarin ICH do not support use of these tests for withholding anticoagulation in patients with atrial fibrillation.]. 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:18845797
;
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:NP702705.RA5QI4nX77qN-hHN_kQHcfOR0-EP9eKX7gw4eSo1k2YH0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}