@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc
> .
@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:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_head
{
this:
np:hasAssertion
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_assertion
;
np:hasProvenance
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_assertion
a
np:Assertion
.
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_provenance
a
np:Provenance
.
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN1368f30850e3086bf2aff17b693af6c9
sio:SIO_000628
miriam-gene:1588
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_provenance
{
dgn-np:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_assertion
dcterms: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:NP46166.RAVs6NByTcSEq4iiYrx_1V36saP6nOwrKdDqzz_OcpJAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}