@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA
> .
@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:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_head
{
this:
np:hasAssertion
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion
;
np:hasProvenance
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance
;
np:hasPublicationInfo
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion
a
np:Assertion
.
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance
a
np:Provenance
.
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGN4666379ed11b1b51f7f4a62943cce15f
sio:SIO_000628
miriam-gene:2153
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_provenance
{
dgn-np:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_assertion
dcterms:description
"[We found no differences in the prevalence of genetic risk factors of thrombosis in women with preeclampsia compared with controls, which makes it unlikely that these polymorphisms are risk factors for 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:15333035
;
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:NP44371.RAaJa8lxDFoUFFapyPMevSPl5gZm3E36JAWhvHLzoxbPA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}