@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM
> .
@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:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_head
{
this:
np:hasAssertion
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion
;
np:hasProvenance
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance
;
np:hasPublicationInfo
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion
a
np:Assertion
.
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance
a
np:Provenance
.
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion
{
miriam-gene:51206
a
ncit:C16612
.
lld:C0019080
a
ncit:C7057
.
dgn-gda:DGN41c76bb770203044da50e050ce88f1f2
sio:SIO_000628
miriam-gene:51206
,
lld:C0019080
;
a
sio:SIO_001122
.
}
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_provenance
{
dgn-np:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_assertion
dcterms:description
"[Cyclooxygenase-1 -842G and 50T alleles significantly contribute to the risk of bleeding complications in patients undergoing elective CAG. Genetic testing is able to influence the safety of diagnostic cardiac catheterization in large numbers of low risk patients with borderline indications.]. 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:20691446
;
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:NP91117.RA5VhV2A0aXRwQJEEUajjBBEua3vq9xHsbptn-CV6QBzM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}