@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk
> .
@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:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_head
{
this:
np:hasAssertion
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_assertion
;
np:hasProvenance
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_provenance
;
np:hasPublicationInfo
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_assertion
a
np:Assertion
.
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_provenance
a
np:Provenance
.
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN0b0688559d709640c05c1a0c840f20bc
sio:SIO_000628
miriam-gene:2099
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_provenance
{
dgn-np:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_assertion
dcterms:description
"[Given the strong genetic contribution to blood pressure and left ventricular hypertrophy (LVH), and the influence of estrogen on these parameters, we hypothesized that polymorphisms in the estrogen receptor alpha (ERalpha) promoter may influence LVH.]. 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:17095210
;
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:NP882253.RAUy24acYlqcMq3DOenHRE22eVTj79ZsssnYA5KsA-esk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}