@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k
> .
@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:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_head
{
this:
np:hasAssertion
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_assertion
;
np:hasProvenance
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_assertion
a
np:Assertion
.
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_provenance
a
np:Provenance
.
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN7e39317dc255a603c7f34556dfe0afa2
sio:SIO_000628
miriam-gene:342977
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_provenance
{
dgn-np:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_assertion
dcterms:description
"[We investigated associations between the NOS3 Glu298Asp SNP (rs1799983) and hypertension, as well as the interaction between NOS3 genotypes and dietary fat intake using data from baseline examination in white and African American participants in the Atherosclerosis Risk in Community (ARIC) study.]. 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:19960019
;
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:NP927319.RA9_VPqgqJ8q-64H6UavDfjINCxZ3e7fo9DOb6sqJgQ5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}