@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_head
{
this:
np:hasAssertion
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion
;
np:hasProvenance
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion
a
np:Assertion
.
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance
a
np:Provenance
.
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C0154208
a
ncit:C7057
.
dgn-gda:DGNe5c0ccb9e167541b0b859973d8cecdc0
sio:SIO_000628
miriam-gene:668
,
lld:C0154208
;
a
sio:SIO_001121
.
}
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_provenance
{
dgn-np:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_assertion
dcterms:description
"[Mutations in FOXL2 are known to cause blepharophimosis syndrome (BPES), an autosomal dominant eyelid malformation associated (type I) or not (type II) with ovarian dysfunction, leading to premature ovarian failure (POF).]. 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:18726931
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP689655.RAywv0nsdE-gtXJ6maybiBMwmhOAo15f0-imx2js0CUIs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:57+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}