@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U
> .
@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:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_head
{
this:
np:hasAssertion
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_assertion
;
np:hasProvenance
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_provenance
;
np:hasPublicationInfo
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_assertion
a
np:Assertion
.
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_provenance
a
np:Provenance
.
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_assertion
{
miriam-gene:2268
a
ncit:C16612
.
lld:C0013537
a
ncit:C7057
.
dgn-gda:DGNb5f9a6b310b25a89ee94871ad0584547
sio:SIO_000628
miriam-gene:2268
,
lld:C0013537
;
a
sio:SIO_001121
.
}
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_provenance
{
dgn-np:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_assertion
dcterms:description
"[We genotyped 6755 mother/infant pairs from the Avon Longitudinal Study of Parents and Children (ALSPAC) to determine whether maternal or fetal FVL or PT, either alone or in combination, are associated with fetal growth restriction (FGR) or pre-eclampsia (PE).]. 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:18752569
;
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:NP456031.RAoQ70USGCr8ppXA_nNo48ciF85N8Mp3dMvjbWPnUd73U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}