@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ
> .
@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:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_head
{
this:
np:hasAssertion
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion
;
np:hasProvenance
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion
a
np:Assertion
.
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance
a
np:Provenance
.
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion
{
miriam-gene:4314
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN03b34e71cedb2af83800fce4c5e0047e
sio:SIO_000628
miriam-gene:4314
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_provenance
{
dgn-np:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_assertion
dcterms:description
"[ There is a low frequency of the stromelysin-1 promoter 5A allele in the Chinese population in Taiwan. How stromelysin-1 5A/6A polymorphism affects ISR appears to be linked to angina status. These results merit further study to identify patients carrying genotypes which put them at increased risk of ISR, and which matrix metalloproteinase inhibitors or drug-eluting stents are more effective for those at risk.]. 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:16323393
;
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:NP54503.RA0FxyzkEpcwCi4q6lYjUJfSIt-7zOiLKQauxeO2bzohQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}