@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q
> .
@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:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_head
{
this:
np:hasAssertion
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion
;
np:hasProvenance
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion
a
np:Assertion
.
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance
a
np:Provenance
.
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion
{
miriam-gene:5468
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN981ad1631eab4285f434452019af3ff9
sio:SIO_000628
miriam-gene:5468
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_provenance
{
dgn-np:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_assertion
dcterms:description
"[The PPARgamma-2 genotype was not associated with an increased or reduced risk of the occurrence of CHD and can therefore not be regarded as an independent risk factor for CHD in patients with diabetes mellitus.]. 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:11916624
;
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:NP592417.RA4yQ3i5mjtMqD5VgybZGklJC4orVQSw8Fk1nuZSfuk8Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}