@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU
> .
@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:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_head
{
this:
np:hasAssertion
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_assertion
;
np:hasProvenance
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_provenance
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np:hasPublicationInfo
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_assertion
a
np:Assertion
.
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_provenance
a
np:Provenance
.
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_assertion
{
miriam-gene:3972
a
ncit:C16612
.
lld:C0162739
a
ncit:C7057
.
dgn-gda:DGN7003822f89d2f280dde3bf34e8eb2c44
sio:SIO_000628
miriam-gene:3972
,
lld:C0162739
;
a
sio:SIO_001121
.
}
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_provenance
{
dgn-np:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_assertion
dcterms:description
"[Out of the 350 differentially expressed genes in preeclampsia and 554 genes in HELLP syndrome, 224 genes (including LEP, CGB, LHB, INHA, SIGLEC6, PAPPA2, TREM1, and FLT1) changed in the same direction (elevated or reduced) in both syndromes.]. 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:20541258
;
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:NP694687.RATuLzVS_UDZxmtPU9UcSYE46nyFKLtxpMiNkMZZL7oSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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
<
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> , <
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" .
}