@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM
> .
@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:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_head
{
this:
np:hasAssertion
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_assertion
;
np:hasProvenance
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_provenance
;
np:hasPublicationInfo
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_assertion
a
np:Assertion
.
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_provenance
a
np:Provenance
.
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_assertion
{
miriam-gene:6404
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNe71c61d4a42fa724a1f639db13c6296e
sio:SIO_000628
miriam-gene:6404
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_provenance
{
dgn-np:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_assertion
dcterms:description
"[We explored the association between PSGL-1 VNTR polymorphisms (especially AB genotype that has the most deformed configuration of the binding site) and the development of coronary stent restenosis and stent thrombosis in patients with coronary artery disease (CAD).]. 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:17221329
;
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:NP785958.RAh_OHwLrVLSfew6DHFjJiRl9GBzANEvUs-bOsSQ7npuM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}