@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE
> .
@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:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_head
{
this:
np:hasAssertion
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion
;
np:hasProvenance
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance
;
np:hasPublicationInfo
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion
a
np:Assertion
.
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance
a
np:Provenance
.
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0085083
a
ncit:C7057
.
dgn-gda:DGNc2cb77c2935c92196e826e0449969a76
sio:SIO_000628
miriam-gene:2153
,
lld:C0085083
;
a
sio:SIO_001121
.
}
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_provenance
{
dgn-np:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_assertion
dcterms:description
"[The results of this study suggest that FVL and PGM presence in asymptomatic women and in the absence of other risk factors do not influence IVF outcome, or represent risk factors for ovarian hyperstimulation syndrome (OHSS), or favour thrombosis after IVF.]. 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:21868400
;
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:NP222599.RAR4foq1IdNPs8MB1dY7DE8ZULu1en8Qw7F-dDkoykFdE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}