@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0
> .
@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:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_head
{
this:
np:hasAssertion
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion
;
np:hasProvenance
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion
a
np:Assertion
.
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance
a
np:Provenance
.
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion
{
miriam-gene:1906
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN1a5d9d3d487cdcbbd709c95c86201035
sio:SIO_000628
miriam-gene:1906
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_provenance
{
dgn-np:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_assertion
dcterms:description
"[In order to investigate the possible association of the -231 G > A polymorphism in the endothelin-1 type A receptor gene (EDNRA), previously shown to be associated with other conditions characterized by vasospasm, we examined 77 Caucasian preeclamptic women and 67 matched controls including normotensive subjects without history of thromboembolic event, abnormalities in blood pressure, proteinuria, edema and preeclampsia.]. 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:17437213
;
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:NP601533.RAWIBf1oGAm8sF0kLMu-m3ddzoZmlqO_9BxMIqkgGNXp0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}