@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY
> .
@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:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_head
{
this:
np:hasAssertion
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_assertion
;
np:hasProvenance
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_provenance
;
np:hasPublicationInfo
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_assertion
a
np:Assertion
.
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_provenance
a
np:Provenance
.
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C1368683
a
ncit:C7057
.
dgn-gda:DGNd0f58853c9b966eeae344c798abc0ed4
sio:SIO_000628
miriam-gene:2492
,
lld:C1368683
;
a
sio:SIO_001121
.
}
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_provenance
{
dgn-np:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_assertion
dcterms:description
"[We previously showed that the expressing level of FSH receptor (FSHR) increased from ovarian epithelial inclusions (OEIs) to benign ovarian epithelial tumors (OETs) and to borderline OETs, whereas FSHR levels decreased with an increase in carcinoma grade.]. 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:19181441
;
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:NP822897.RAxneUpN7N12kN_souoX3RenuUxDipoI1A1WOdL_uy3YY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}