@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0
> .
@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:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_head
{
this:
np:hasAssertion
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_assertion
;
np:hasProvenance
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_provenance
;
np:hasPublicationInfo
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_assertion
a
np:Assertion
.
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_provenance
a
np:Provenance
.
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_assertion
{
miriam-gene:64805
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN5d0ea01a0058df66c030068b71f40a08
sio:SIO_000628
miriam-gene:64805
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_provenance
{
dgn-np:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_assertion
dcterms:description
"[The H2 haplotype of the P2RY12 was determined in 1378 unrelated patients of both sexes selected according to the presence of significant coronary artery disease (CAD group) or having normal coronary angiogram at cardiac catheterization (CAD-free group).]. 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:17803810
;
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:NP215846.RAidqgL4UHEBKzUOOhu3_tUVK_3T8MCzo6ZEeuPzNGFY0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}