@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4
> .
@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:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_head
{
this:
np:hasAssertion
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion
;
np:hasProvenance
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion
a
np:Assertion
.
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance
a
np:Provenance
.
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGN7dd6f5cda721398c121e4c7fe43d4f38
sio:SIO_000628
miriam-gene:348
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_provenance
{
dgn-np:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_assertion
dcterms:description
"[ We were unable to demonstrate that the atherogenic state of preeclampsia is associated with a particular genotype of apo E. Familial studies show that shared genetic and environmental factors are involved in lipid variability. However, owing to the diversity of factors contributing to the development of preeclampsia (fetal and paternal genotypes), these data do not allow to rule-out a possible contribution of maternal apo E to 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:12175441
;
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:NP48310.RAIrhd9YyUtate9-DZz9yxZoCt3X7w7dRGavdiLb8pjK4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}