@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0
> .
@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:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_head
{
this:
np:hasAssertion
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_assertion
;
np:hasProvenance
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_assertion
a
np:Assertion
.
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_provenance
a
np:Provenance
.
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN287a5fd1f957f33e56d571dacfc6b32a
sio:SIO_000628
miriam-gene:2908
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_provenance
{
dgn-np:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_assertion
dcterms:description
"[A single-nucleotide polymorphism (SNP) in the human glucocorticoid receptor (hGR) N363S (rs6195) has been the focus of several clinical studies, and some epidemiological data link this SNP to increased glucocorticoid sensitivity, coronary artery disease, and increased body mass index.]. 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:17535992
;
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:NP784205.RAIRkQDweNJkHiTzA3mkqcs6ecjb2f_CD4LlvHQOvbTK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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" .
}