@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk
> .
@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 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:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_head
{
this:
np:hasAssertion
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion
;
np:hasProvenance
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance
;
np:hasPublicationInfo
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion
a
np:Assertion
.
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance
a
np:Provenance
.
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN0adb4cf9e72593c2316220599e4f927d
sio:SIO_000628
miriam-gene:367
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance
{
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion
dct:description
"[The purpose of this study was to analyse the frequency and type of mutations in the coding region of androgen receptor (AR) and to determine the role of polymorphisms in the intron 1 of ERalpha, exon 5 of ERbeta, intron 7 of progesterone, exon 7 of the aromatase (CYP19) and exon 9 of VDR genes in the risk of prostate cancer.]. 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:18483761
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}