@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ
> .
@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:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_head
{
this:
np:hasAssertion
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_assertion
;
np:hasProvenance
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_assertion
a
np:Assertion
.
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_provenance
a
np:Provenance
.
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_assertion
{
miriam-gene:2001
a
ncit:C16612
.
lld:C0032962
a
ncit:C7057
.
dgn-gda:DGNa7e829cf31249f7a4513073c41b4be36
sio:SIO_000628
miriam-gene:2001
,
lld:C0032962
;
a
sio:SIO_001121
.
}
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_provenance
{
dgn-np:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_assertion
dcterms:description
"[Our identification of the trophoblast-specific transcriptional circuit established by ELF5 will be instrumental to derive human TS cell lines that truly reflect early placental trophoblast and that will be most beneficial to gain insights into the aetiology of common pregnancy complications, including intra-uterine growth restriction and pre-eclampsia.]. 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:20354077
;
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:NP860933.RAoF-M4kLQwIGH6zCSA27Qcq8AmRyOpEB3jDImKj0ZhMQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:46+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" .
}