@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_head
{
this:
np:hasAssertion
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_assertion
a
np:Assertion
.
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_provenance
a
np:Provenance
.
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_publicationInfo
a
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.
}
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN609cc27d15fdb273e1253fac8a8224a2
sio:SIO_000628
miriam-gene:7421
,
lld:C0376358
;
a
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.
}
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_provenance
{
dgn-np:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_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-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP123157.RAapKErfVR-MchM5MQSh6O4_FUns0Br3eR3ZZOuGUHWXw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:43+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
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;
pav:authoredBy
<
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> , <
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
}