@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ
> .
@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:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_head
{
this:
np:hasAssertion
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_assertion
;
np:hasProvenance
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_assertion
a
np:Assertion
.
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_provenance
a
np:Provenance
.
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0856169
a
ncit:C7057
.
dgn-gda:DGN0731c5bd87a36ea94fb44af8f38d509c
sio:SIO_000628
miriam-gene:342977
,
lld:C0856169
;
a
sio:SIO_001121
.
}
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_provenance
{
dgn-np:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_assertion
dcterms:description
"[Since patients with the metabolic syndrome are known to have endothelial dysfunction, we aimed to investigate if the significance of NOS3 polymorphisms may depend on the presence of the metabolic syndrome.]. 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:19407362
;
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:NP548490.RAj43QZGOzFZMiV29t9WYbS_vFwRa6EUd6NgRYHdmPvfQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}