@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4
> .
@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:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_head
{
this:
np:hasAssertion
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_assertion
;
np:hasProvenance
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_assertion
a
np:Assertion
.
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_provenance
a
np:Provenance
.
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_assertion
{
miriam-gene:5104
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN84ff930fe4491a835c6275457fddce43
sio:SIO_000628
miriam-gene:5104
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_provenance
{
dgn-np:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_assertion
dcterms:description
"[The hypothesis was tested by screening for the prevalence of the above polymorphisms in 201 coronary artery disease (CAD) patients subjected to PCI and presenting with symptoms or signs of recurrent ischemia.]. 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:19404719
;
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:NP666526.RAvBqsQN06ichoOrrZ816Eq4BrKbSHaykeDXR4qPjWAX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}