@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg
> .
@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:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_head
{
this:
np:hasAssertion
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_assertion
;
np:hasProvenance
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_assertion
a
np:Assertion
.
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_provenance
a
np:Provenance
.
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGN432f7b3dd247a929255fb44ab654a6b9
sio:SIO_000628
miriam-gene:4846
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_provenance
{
dgn-np:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_assertion
dcterms:description
"[ These data provide evidence for an association between NOS3 and preeclampsia. In defined ethnic groups, this NOS3 may offer predictive information regarding the subsequent development of preeclampsia and its clinical course.]. 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:12044319
;
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:NP61716.RACpNbENgRFQ-1VkI6gE6biWbgMbjNw20nOPD2CA4cTxg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}