@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ
> .
@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:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_head
{
this:
np:hasAssertion
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_assertion
;
np:hasProvenance
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_assertion
a
np:Assertion
.
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_provenance
a
np:Provenance
.
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_assertion
{
miriam-gene:1022
a
ncit:C16612
.
lld:C0340288
a
ncit:C7057
.
dgn-gda:DGNf7053a63de956d5c50d645790ba64f68
sio:SIO_000628
miriam-gene:1022
,
lld:C0340288
;
a
sio:SIO_001121
.
}
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_provenance
{
dgn-np:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_assertion
dcterms:description
"[The results showed that the expression of TLR4 and MAPK families are increased in the patients with acute coronary syndrome (ACS), compared with it in the patients with stable angina and controls.]. 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:18373609
;
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:NP678135.RAdiqf8hawSOVF-CpJBEZIw6R5eD5WHKiDdpnP4NVo0cQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}