@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ
> .
@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 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:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_head
{
this:
np:hasAssertion
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion
;
np:hasProvenance
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion
a
np:Assertion
.
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance
a
np:Provenance
.
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion
{
miriam-gene:1576
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNf6f8fe3337870c2462fb20f5ed6236d3
sio:SIO_000628
miriam-gene:1576
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance
{
dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion
dct:description
"[The CYP3A5 genotype was related with blood pressure in the general population, but the effect on the risk for hypertension in pregnancy has not been evaluated.We compared the allele and genotype frequencies of three functional SNPs in the CYP3A5 (rs776746), CYP3A4 (rs2740574), and CYP21A2 (rs6471) genes between pregnant women who developed hypertension (n = 250) or who remained normotensive (control group, n = 250).]. 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:20617557
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}