@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ
> .
@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:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_head
{
this:
np:hasAssertion
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_assertion
;
np:hasProvenance
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_assertion
a
np:Assertion
.
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_provenance
a
np:Provenance
.
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_assertion
{
miriam-gene:5104
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNc05b34348c41fa1e2164a66617d683a7
sio:SIO_000628
miriam-gene:5104
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_provenance
{
dgn-np:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_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:NP702117.RAjgH5efRTS7QFW5r4hYQvBolY5iFkaKwx7us5KAZ2WEQ130_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" .
}