@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs
> .
@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:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_head
{
this:
np:hasAssertion
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_assertion
;
np:hasProvenance
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_provenance
;
np:hasPublicationInfo
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_assertion
a
np:Assertion
.
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_provenance
a
np:Provenance
.
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNb5978f55ceb267b737cb260affd0bb85
sio:SIO_000628
miriam-gene:1756
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_provenance
{
dgn-np:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_assertion
dcterms:description
"[Logistic regression analysis showed that the presence of Fx and of AH and the combination of the presence of Fx plus AH were associated with the H2 genotype regardless of the degree of cortisol secretion, age, BMI and BMD (OR 4.88, 95%CI 1.47-18.40, P = 0.05; OR 8.25, 95%CI 0.98-69.52, P = 0.05; OR 7.25, 95%CI 1.57-35.78, P = 0.011; respectively).]. 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:20584071
;
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:NP589074.RAPvTTgDJq8BnSFf9blVPMC3gel44W0nY0qO5arB7h_cs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}