@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8
> .
@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:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_head
{
this:
np:hasAssertion
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_assertion
;
np:hasProvenance
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_provenance
;
np:hasPublicationInfo
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_assertion
a
np:Assertion
.
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_provenance
a
np:Provenance
.
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_assertion
{
miriam-gene:668
a
ncit:C16612
.
lld:C1862261
a
ncit:C7057
.
dgn-gda:DGN9f480eb2bd69feeaabae0261dde71eab
sio:SIO_000628
miriam-gene:668
,
lld:C1862261
;
a
sio:SIO_001121
.
}
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_provenance
{
dgn-np:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_assertion
dcterms:description
"[In contrast to known FOXL2 mutations with polyalanine expansions and association with BPES type II, clinical aspects of our girl may indicate some degree of ovarian dysfunction that might finally lead to BPES type I with premature ovarian failure.]. 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:16131596
;
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:NP520560.RAz6lfnav2n66vkhNWecTu2ltoYt1-Xwy6aGJvgYdSQk8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}