@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco
> .
@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:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_head
{
this:
np:hasAssertion
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_assertion
;
np:hasProvenance
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_provenance
;
np:hasPublicationInfo
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_assertion
a
np:Assertion
.
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_provenance
a
np:Provenance
.
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_assertion
{
miriam-gene:729230
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN8fe22cfb86f44fdc1d0ef666163a31cd
sio:SIO_000628
miriam-gene:729230
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_provenance
{
dgn-np:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_assertion
dcterms:description
"[Although we could not detect any association of CCR2 polymorphic markers with CAD, several SNP markers of CCR2 gene showed highly significant signals with the number of arteries with significant coronary artery stenosis in the CAD male patients.]. 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:17482150
;
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:NP63909.RA1FBYESMWQ-72TGSRmeys-CAiO8POoDaHmWIeoTuZcco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}