@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o
> .
@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:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_head
{
this:
np:hasAssertion
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_assertion
;
np:hasProvenance
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_assertion
a
np:Assertion
.
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_provenance
a
np:Provenance
.
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0010481
a
ncit:C7057
.
dgn-gda:DGN8ca0d63b0f3bd6f4b1c7a65af29abe17
sio:SIO_000628
miriam-gene:1756
,
lld:C0010481
;
a
sio:SIO_001121
.
}
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_provenance
{
dgn-np:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_assertion
dcterms:description
"[The aim of the present study was to explore presumed associations between the 83,557insA variant of the HSD11B1 gene and circulating hormone concentrations, bone turnover and bone mineral density (BMD) in patients with endogenous Cushing's syndrome (CS).]. 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:21111044
;
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:NP411220.RAuN6BXvpcaS2E9WIJQm7vN_uF69Yzyce9e6q6VTiS4-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}