@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E
> .
@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:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_head
{
this:
np:hasAssertion
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_assertion
;
np:hasProvenance
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_assertion
a
np:Assertion
.
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_provenance
a
np:Provenance
.
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGN5579bc5d7786cfd19b5b511bcc2f1771
sio:SIO_000628
miriam-gene:4846
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_provenance
{
dgn-np:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_assertion
dcterms:description
"[ These genotype data in subjects from eastern Finland were not suggestive of an important contribution of the Glu298Asp polymorphism in the NOS gene on preeclampsia across populations. However, the observed association between the G allele and disease risk, of borderline significance, may imply that other polymorphism(s) in the gene may modify disease risk.]. 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:12699878
;
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:NP61715.RAFF0SwjR-Mw_HM6OBhbd_ezwtdu8KLxRwiO-DpAnek2E130_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" .
}