@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc
> .
@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:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_head
{
this:
np:hasAssertion
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_assertion
;
np:hasProvenance
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_provenance
;
np:hasPublicationInfo
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_assertion
a
np:Assertion
.
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_provenance
a
np:Provenance
.
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_assertion
{
miriam-gene:1524
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNcc8de5aec1270534ccaed15f153a79b2
sio:SIO_000628
miriam-gene:1524
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_provenance
{
dgn-np:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_assertion
dcterms:description
"[In the present CAD population, no differences in circulating levels of fractalkine or expression levels of CX3CR1 were observed between patients with and without T2DM, or with and without metabolic syndrome, which may be related to their underlying disease.]. 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:22897138
;
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:NP229331.RAwW1MfG2XJ13tOQjY_GBfqqeXGMu18S28_h_XWz9nrzc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}