@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA
> .
@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:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_head
{
this:
np:hasAssertion
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_assertion
;
np:hasProvenance
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_provenance
;
np:hasPublicationInfo
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_assertion
a
np:Assertion
.
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_provenance
a
np:Provenance
.
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_assertion
{
miriam-gene:30816
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGNc8c1d2e92eafeb161218c0c735a6e2a5
sio:SIO_000628
miriam-gene:30816
,
lld:C0032914
;
a
sio:SIO_001123
.
}
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_provenance
{
dgn-np:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_assertion
dcterms:description
"[contributor to normal placental architecture, especially in the fusion processes of cytotrophoblasts to syncytiotrophoblasts.the gene expression of syncytin may be altered in cases with placental dysfunction such as preeclampsia or HELLP syndrome.]. 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:11854637
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP131745.RAxc3Zbm9gczG0_v9NY5YOwdsbXTIL99kTlS8O3NTICjA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:08+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" .
}