@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4
> .
@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:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_head
{
this:
np:hasAssertion
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_assertion
;
np:hasProvenance
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_provenance
;
np:hasPublicationInfo
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_assertion
a
np:Assertion
.
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_provenance
a
np:Provenance
.
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN617347d9ccf6b112b8c47711c956d986
sio:SIO_000628
miriam-gene:7450
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_provenance
{
dgn-np:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_assertion
dcterms:description
"[Prominent features of OHSS are an elevated risk of thromboembolism due to enhanced production of von Willebrand factor by endothelial cells and ascites, or pulmonary edema due to increased vascular permeability followed by third space fluid accumulation.]. 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:7775647
;
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:NP504553.RAUU7yEtsY5t_bVlEP5nj9A7XENhWz3ujKIoosYilVVv4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}