@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY
> .
@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:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_head
{
this:
np:hasAssertion
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_assertion
;
np:hasProvenance
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_provenance
;
np:hasPublicationInfo
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_assertion
a
np:Assertion
.
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_provenance
a
np:Provenance
.
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGNa3323df0bc19d6f609ab236cd61c0f09
sio:SIO_000628
miriam-gene:3643
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_provenance
{
dgn-np:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_assertion
dct:description
"[The lack of an association between preeclampsia and the polymorphisms studied suggests that other genes whose products do not have direct functional interaction with metabolic syndrome or epigenetic factors may play a role in 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:18716398
;
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:NP71802.RAQ2kBaEsbZyQ4mxoPofAhJPSRpHn8q0h8TWt8xkN41nY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:35+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" .
}