@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g
> .
@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:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_head
{
this:
np:hasAssertion
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_assertion
;
np:hasProvenance
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_provenance
;
np:hasPublicationInfo
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_assertion
a
np:Assertion
.
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_provenance
a
np:Provenance
.
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_assertion
{
miriam-gene:2268
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNb8143357a25e0811d344b0917418c133
sio:SIO_000628
miriam-gene:2268
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_provenance
{
dgn-np:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_assertion
dcterms:description
"[To determine to what extent double inherited thrombophilias are associated with adverse obstetric complications correlated with fetoplacental insufficiency, such as preeclampsia, hemolytic anemia elevated liver enzymes and low platelet count (HELLP) syndrome, gestational hypertension, fetal growth restriction (FGR), intrauterine death (ID), abruptio placentae and disseminated intravascular coagulopathy.]. 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:20868443
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP537101.RAMP2sjbiYm2qnNKqnjDlSkHJwZ4fqimAOtNVqpltBJ0g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}